Cyproheptadine Hcl offered by us white or slightly yellow, odorless or practically odorless, crystalline powder. Our range is an antihistaminic, ant cholinergic and antiserotonergic agent that acts as a 5-HT2 receptor antagonist. These are 4-(5H- Dibenzo cycloheptan- 5-ylidene)-1- methylpiperidine hydrochloride and are used to treat allergic reactions. Our range also stimulates appetite in underweight people. Besides, these are slightly soluble in water, freely soluble in methanol, soluble in chloroform, sparingly soluble in alcohol and practically insoluble in ether.
 
Following are the salient features of our range:

• Preventative measure against migraine in children and adolescents
• Used in cats as an appetite stimulant
• Treatment of asthma
• Relieve SSRI-induced sexual dysfunction
• Molecular Weight :  350.88

Technical specifications of our range are as follows:
 

PRODUCT NAME : CYPROHEPTADINE HCL
Chemical Name :	4-(5H-DIBENZO[a,d]CYCLOHEPTAN- 5-YLIDENE)-1-METHYLPIPERIDINE HYDROCHLORIDE
Molecular Formula :	C21H21N•HCl• 1 1/2H2O
Molecular Weight :	350.88
CAS No.	[41354-29-4]
TEST	STANDARDS
Description	White or slightly yellow, odorless or practically odorless, crystalline powder
Solubility	Slightly soluble in water, freely soluble in methanol; soluble in chloroform; sparingly soluble in alcohol; practically insoluble in ether.
Identification	A) By Infra red spectrophotometry B) By Ultra violet spectrophotometry C) TLC. D) Reaction of Chloride
Acidity	NMT - 0.15 ml of 0.1N NaOH solution
Water	Between 7.0% – 9.0%
Sulphated Ash	Not more than 0.1%
Related Substances	Dibenzocycloheptene : NMT 0.2% Any other spot : NMT 0.1%
Assay (on Anhydrous Basis)	Between 98.5% - 101.0%

We offer amlodipine base or besilate that is used as an anti-hypertensive and in the treatment of angina. These are white to off crystalline powder and are soluble in methanol. Our range reduces blood pressure as well as increases blood flow to the heart muscle.

Following re the technical specifications of our range:

• Chemical Name: `3-Ethyl-5-Methyl-(4-RS)-2-[(2-AminoEthoxy) Methyl]-4-(2- Chlorophenyl)-6-Methyl-1-4-Dihydro-Pyridine-3, 5-DiCarboxylate
• Description: White to off White Crystalline powder
• Solubility: Soluble in methanol
• Water Content: Not more than 0.5%
• Identification by HPLC:            Sample retention time should match with standard retention time
• Related Substances by HPLC:  Impurity D: Not more than 0.30%, Highest unknown impurity: NMT 0.50%nd Total Impurities: NMT 1.00%
• Assay by HPLC: (On dry basis) not less than 99.00%

We formulate lidocain Hcl that is clear & colorless solution and is offered to fulfill the varied requirements of pharma & chemical industries. Our range of Lidocain Hcl is an   anesthetic and antiarrhythmic drug that is used to relieve itching, burning & pain from skin inflammations. Besides, these are also injected as a dental anesthetic and in minor surgeries.

Following are the technical specifications of lidocain Hcl:

PRODUCT NAME : Lidocain Hcl
TEST	STANDARDS
Description	White crystalline powder
Solubility	Complies
Identification	A. Melting Point - 76 O C B. IR Spectrum - Complies C. Melting Point - 229 O C D. Color Test - Complies E. Color Test - Complies F. Chloride Test - Complies
Appearance of Solution	Clear and colorless
pH	5.32
Impurity (A)	Less than 100 ppm
Heavy Metals	Less than 5 ppm
Water Content	6.26%
Sulphated Ash	0.058%
Assay (On anhydrous Basis)	99.65%

We offer citalopram Hbr that is off white to white powder that is free from strange matter. These are soluble in acetone as well as in water and are available as tablets or as an oral solution. These are widely used in various pharma & chemical industries and have the following technical specifications:

• Chemical Name: 1-[3-(Dimethylamino) propyl] –1-(4 – fluorophenyl) –1, 3–dihydro – 5 –iso bezofuran carbonitrile. Hydrobromide

• Description: An Off white to white powder free from strange matter
• Solubility: Soluble in Acetone and in Water
• Identification:

A) By I.R.
B) Melting Range (182oc to 188.0oc)
C) Test for Bromide (Positive)

• Loss on drying: Not more than 0.5% w/w
• Sulphated ash: Not more than 0.1%
• Heavy Metals: Not more than 20 ppm
• Related substances by HPLC: Single impurity : Not more than 0.5 %, Total Impurities : Not more than 1.0 %
• Assay (By Chemical on dried basis): Not more than 0.5%

We are engaged in offering of Atenolol that is white powder and is sparingly soluble in water; soluble in ethanol, slightly soluble in methylene chloride & practically insoluble in ether. Our range is a β1 receptor selective antagonist that means a drug belonging to the group of β-blockers and is widely used for treating cardiovascular diseases. Besides, our range is also used for curing hypertension as well as the symptoms of graves diseases.

PRODUCT NAME : Atenolol BP
TEST	STANDARDS
Description	White to Almost white powder.
Solubility	Sparingly soluble in water; soluble in ethanol, slightly soluble in methylene chloride; Practically insoluble in ether.
Identification	Complies with BP test B, C & D
Melting range	Between 152°C to 155°C
Appearance of Solution	The solution is clear and not more than intensely colored than degree 6 of the range of reference solution of the most appropriate color.
Optical Rotation (at 20oc)	Between +0.10°C to –0.10°C
Chlorides	NMT 0.1%
Related Substances Individual Impurity Total Impurities	NMT 0.25% NMT 0.50%
Sulphated Ash	NMT 0.1%
Loss On Drying (At 105oC)	NMT 0.5%
Assay (On dried basis)	Between 99.0% - 101.0%

  

Cisapride offered by us is a white powder and acts as a serotonin 5-HT4 receptor. Our range helps in stimulation of serotonin receptors and increases acetylcholine release in the enteric nervous system. Our range is practically insoluble in water, freely soluble in DMF, soluble in methylene chloride and sparingly soluble in methanol.

It shows polymorphism and has the following benefits:

• Increases muscle tone in the esophageal sphincter
• Increases gastric emptying in people with diabetic gastro paresis
• It has been used to treat bowel constipation
• It is also prescribed by veterinarians for curing hair balls in cats

Technical specifications of cisapride are as follows:

 

PRODUCT NAME : CISAPRIDE MONOHYDRATE
Chemical Name :	-cis-4-amino-5-chloro-N-[1-[3-(4-fluorophenoxy) propyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamide monohydrate
TEST	STANDARDS
Description	A white or almost white powder
Solubility	Practically insoluble in water, Freely soluble in DMF, Soluble in Methylene chloride, Sparingly soluble in methanol. It shows polymorphism
Identification IR	The spectrum obtained with the substance to be examined correspond in position and relative size to those in the spectrum obtained with Cisapride monohydrate reference standard (working standard)
Appearance of the solution	Not more intensely colored than ref solution BY6
Related Substances by HPLC	Single Impurity: NMT 0.5% Total Impurity : NMT 1.0%
Optical Rotation	Between -0.1° to +0.1°
Heavy metals	Not more than 20PPM
Water	Between 3.4 to 4.0% w/w
Sulphated Ash	Not more than 0.10% w/w
Assay (By chemicals)	NLT 99.0 % w/w and NMT 101 % w/w

Fexofenadine Hcl offered by us is whit crystalline powders that is soluble in methanol & dilute NaOH.  Their molecular weight is 538.13 and the empirical formula is C32H39NO4•HCl. Our range of fexofenadine is a racemate and exists as a zwitterion in aqueous media at physiological pH. These are identified by I.R. spectrophotometry and have the following technical specifications of fexofenadine Hcl:
 

PRODUCT NAME : : FEXOFENADINE HCL
TEST	STANDARDS
Description	White crystalline powder.
Solubility	Soluble in methanol and dilute NaOH
Identification	By I.R. Spectrophotometry
Loss on Drying	Not more than 1.0 %
Melting range	Between 191°C to 198°C
Heavy metals	Not more than 20 ppm
Sulphated ash	Not more than 0.1%
Related Substances by HPLC	Single Impurity: NMT - 0.50% Total Impurity: NMT – 1.0%
Assay by Potentiometer	Between 98.0% - 102.0% (On dried basis)

We are well known for formulating itraconazole that is practically insoluble in water, freely soluble in methylene chloride, sparingly soluble in tetrahydrofuran and very slightly soluble in alcohol. Our range is a triazole antifungal agent that is recommended for treating fungal infections. These also reduce the fungal cytochrome P450 oxidase-mediated synthesis of ergosterol and have the following technical specifications:
 

PRODUCT NAME : ITRACONAZOLE – E.P.
Chemical Name :	2-butan-2-yl-4-[4-[4-[4-[[2-(2,4-dichlorophenyl)-2-(1,2,4-'triazol-1-yl methyl)-1,3-dioxolan-4-yl]methoxy] phenyl]piperazin-1-yl]phenyl]-1,2,4-triazol-3-one
TEST	STANDARDS
Description	A white or almost white powder
Solubility	Practically insoluble in water, freely soluble in methylene chloride, sparingly soluble in tetrahydrofuran and very slightly soluble in alcohol.
Identification	First Identification      (B) Second Identification A,C,D
A) Melting range	Between 166.0°C and 170.0°C
B) IR absorption	The IR absorption spectrum of the sample should match with the spectrum of the Itraconazole working standard.
C) TLC	The principle spot in the chromatogram obtained with the test solution is similar in position, color and size to the principle spot in the chromatogram obtained with reference solution (a) and reference solution (b) shows two clearly separated spots.
D) Chlorides	White crude precipitate observed which is easily dissolved in excess of ammonia solution.
Clarity and appearance of solution	10% w/v solution in Methylene chloride should be clear and not more intensely colored than reference solution BY6
Optical rotation (10% in Methylene chloride)	-0.10°C to +0.10°C
Related substances (By HPLC)	Any single impurity : NMT 0.50% Total impurities : NMT 1.25%
Loss on drying (100 to 1050C for 4 hrs)	NMT 0.50% w/w
Sulphated ash	NMT 0.10% w/w
Assay (on dried basis)	NLT 98.5% and NMT 101.5% w/w

We offer omeprazole powder that is a proton pump inhibitor (PPI) and sodium bicarbonate combination that is widely used for decreasing the amount of acid produced in the stomach. Our range is also used for treating heartburn of the esophagus caused due to gastroesophageal reflux disease. Besides, our range is applicable for short-term treatment of ulcers of the stomach or small intestines. Our range of omeprazole powder is slightly soluble in water, soluble in methylene chloride, sparingly soluble in methanol and in alcohol.

Following are the technical specifications of omeprazole powder:
 

PRODUCT NAME : OMEPRAZOLE POWDER
TEST	STANDARDS
Chemical name	(R,S)-5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl) methyl]sulfinyl]- 1H-benzimidazole, monosodium salt.
Cas No.	95510-70-6
Chemical formula	C17H18N3O3S•Na
Molecular Weight	366.82
Description	A White or almost white powder
Solubility	Very slightly soluble in water, Soluble in Methylene Chloride, sparingly soluble in Methanol and in alcohol, it dissolves in diluted solutions of Alkali Hydroxides.
Identification	A) The 0.002% solution in 0.1N NaOH shows two absorption maxima at 276nm and 305nm and ratio is 1.6 to 1.8. B) The IR spectrum concordant with the spectrum of Omeprazole CRS. C) The spot obtained by TLC is similar in position and size to the Omeprazole CRS
Appearance of Solution	2% solution in MDC is clear.
Absorbance	Absorbance of 2% w/v solution in MDC at 440nm should be Not more than 0.10.
Loss on Drying at 60oc for 4 hrs under vacuum	Not more than 0.2 % W/W
Sulphated Ash	Not more than 0.1 % W/W
Omeprazole impurity ‘C’	By TLC NMT 0.1%
Related Substances by HPLC	Not more than 0.1%
Residual solvents By Head-space gas Chromatography	Chloroform : NMT 50PPM Methylene Chloride : NMT 100PPM
Assay (On dry basis)	NLT 99 % to NMT 101 %

We offer lansoprazole that is a proton pump inhibitor used for preventing the stomach from producing acid. It can melt with decomposition around 166°C and is freely soluble in dimethyl formamide, soluble in methanol, sparingly soluble in ethanol, slightly soluble in ethyl acetate, dichloromethane and acetonitrile. Lansoprazole offered by us is stable when exposed to light for up to two months. Following are the technical specifications of lansoprazole:
 

PRODUCT NAME : LANSOPRAZOLE POWDER
Chemical name :	2-[[[3-methyl-4-(2,2,2-trifluroethoxy)-2-pyridyl]methyl]sulfinyl] benzimidazole
TEST	STANDARDS
Description	A white or almost white powder.
Identification a) By IR b) By UV (1% w/v in methanol)	To be concordant with the working standard. The maximum absorbance wave length should be same as that of working standard..
Water Content by KF	Not more than 0.1 %
Residue on ignition	Not more than 0.1 %
Chromatographic purity ( By HPLC)	a) Related compound A : NMT 0.4% b) Impurity B : NMT 0.1% c) Impurity C : NMT 0.1% d) Other individual impurity : NMT 0.1% e) Total Impurities: Not more than 0.6 %
Residual solvents	a) Iso propyl alcohol : NMT 5000 PPM b) Acetone : NMT 5000 PPM c) N-Hexane : NMT 0290 PPM d) Chloroform : NMT 0060 PPM
Assay by HPLC	Not less than 99 % and Not more than 101% on anhydrous basis

Sildenafil citrate offered by us is white to off-white crystalline powder that is widely used to treat erectile dysfunction and pulmonary arterial hypertension. These are also effective in the rare diseases such as pulmonary arterial hypertension and have melting range of 188°C to 196°C.

Following are the technical specifications of sildenafil citrate:
 

PRODUCT NAME : SILDENAFIL CITRATE
TEST	STANDARDS
Chemical name	1-[[3-(6,7-Dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo [4,3-d] pyrimidin-5-yl)-4- ethoxyphenyl] sulphonyl]-4-methylpiperazine citrate
Description	White to off-White crystalline powder
Solubility	Soluble in DMF
Identification	A. IR Spectrum of sample shall be in Concordant with that of standard B. Test of chloride
Water Content	NMT 3.0%
Loss on Drying	Not more than 0.50% w/w
Sulphated Ash	Not more than 0.2% w/w
Melting Range	188°C to 196°C
Heavy metals	Not more than 20 ppm
Citric Acid Content	Between 28% to 32%
Related Impurity (By HPLC)	Individual Impurity – NMT 0.5% Total Impurity – NMT 1.0%
Assay by HPLC	Between 98.0% - 102.0%(on dried basis)
Assay by Chemical	Between 98.0% - 102.0%(on dried basis)

We are also well known for offering caffine anhydrous that is bitter, white crystalline xanthine alkaloid that acts as a psychoactive stimulant drug and a mild diuretic. In humans, caffeine is a central nervous system stimulant, having the effect of provisionally warding off sleepiness and returning alertness.