Pharmaceutical Medicines

We manufacture and supply ciprofloxacin injection of supreme quality.

COMPOSITION:
Each ml contains :

• Ciprofloxacin 2 mg
• Sodium chloride 0.9%w/v
• Water for injection q.s

CATEGORY: Antibacterial
Floroquinolone antibiotic. Bacterial mode of action.

INDICATIONS: Respiratory tract, Urinary tract, E.N.T., Skin and soft tissues, gastro intestinal tract, intra abdominal gynaenological. Bon and joint and severe systematic infections Gonorrhoea.Ciprofloxacin 400 mg/200 ml IV infusion 12 hourly is indicated for systemic infection, lower respiratory tract infections skin and skin structure infections, typhoid fever, severe complicated urinary tract infections, surgical procedure.

DOSAGE: As Directed by Physician.
STORAGE: Single dose container.

ADVERSE EFFECTS: Hypersenstivity and skin reactions have been associated with Ciprofloxacin and other floroquinolones. Reports have included anaphylaxis(which has been fatal) , serum sickness, toxic epidermal necrolysis.

PRECAUTIONS: Use with caution in patients of renel impairment, cerebral arteriosclerosis or epilepsy.Keep patient well hydrated toprevent crystalluria.

We are one of the leading names in manufacturing , supplying and exporting of metronidazole injection.

Composition :
Each 100ml contains:

• Metronidazole 500 mg
• Sodium Chloride 0.8%w/v
• Water for Injecion q.s
  

INDICATIONS & DOSAGES :
Anaerobic Infections:

Adult: 500mg infused as100ml of a 5 mg/ml solution at 5 ml/min 8 hrly.
Alternatively,15 mg/kg infusion followed by 7.5 mg/kg infusion followed by 7.5 mg/kg 6 hrly; infuse over 1 hr(max ; 4gm in 2 hr).Subtitute oral therapy as soon as possible.

Child: 7.5 mg/kg 8 hrly. Elderly :use lower end of adult dose recommendations. Do not admin as single dose.

PREVENTION OF POST OPERATIVE ANAEROBIC BACTERIAL INFECTIONS:

Adult 500 mg by IV infusion shortly before operation and repeated hrly; oral doses of 200 mg or 400 mg 8 hrly being substitute as soon as possible. Patient undergoing colorectal surgery; 15mg/kg infused over 30 -60 min, completed about 1 hr prior to surgery, followed by 2 further IV doses of 7.5 mg/kg  infused at 6 and 12 hr after the initial dose.

Elderly : Use lower end of adult dose recommendations . Do not admin as single dose.

CONTRA-INDICATIONS: Neurological disease, blood dyscrasias, fist trimester of pregnancySIDE-EFFECTS: Anorexia, nausea metallic taste, abdominal cramps headache,glossitis, dryness of mouth, dizziness, peripheral neuropathy, CNS effects, seizures. Thromboflebitis of injected vein.

The Levofloxacin is used for acute and chronic infections that are caused by sensitive bacteria.

This levofloxacin is effective on the following infections:
 

• Urinary
• Reproductive
• Digestive
• Skin soft
• Tissue
• Respiratory infections
• Gastrointestinal infections
• Typhoid
• Fever
• Bone and joint infections
• Septicemia
• General infections

Composition
Each 100ml contains
Levofloxacin Hemihydrate 
eq. to Levofloxacin............ 500mg
Dextrose(Anhydrous)IP....... 5%w/v
Water for Injection IP...........q.s

Dosage: As directed by the physician

Dextrose is sterile, nonpyrogenic, isotonic and contains no bacteriostatic or antimicrobial agents and is used for intravenous administration. Each 25% Dextrose Injection offers calories is a source of water for hydration. This induces diuresis with respect to the volume administered and the clinical condition of the patient. It can easily metabolized and reduces protein and nitrogen loss in the body. This promotes glycogen deposition and
prevents ketosis.
 
Specifications:
 

• Generic Name: dextrose monohydrate
• Dosage Form: injection
• Partial Fill
• Dextrose Injection Description

Each ml of 25% Dextrose Injection USP contains:
 

• Hydrous Dextrose USP 25 mg
• Water for Injection USP qs
• pH: 4.5 (3.5, 6.5)
• Calculated Osmolarity: 250 mOsmol/liter
• Calories per 100 mL 17

 
This medicine is used in adults and pediatric patients as sources of calories and water for hydration. It can also be used as diluent and delivery system in case of intermittent intravenous administration of compatible drug additives.

We manufacture 100ml pack size of ofloxacin injection that is of supreme quality.

COMPOSITION:

Each ml contains:

• Ofloxacin USP 2 mg
  
• Sodium Chloride 0.9%w/v
  
• Water for injection q.s.
  
• Pack size 100 ml

CATEGORY: Quinolone antibiotic. Antibacterial action.

INDICATIONS: Genito urinary, respiratory, Gastro intestinal, Skin and soft tissue infections. Peritonitis. Gonorrhoea.

DOSAGE: For Intravenous infusion only 2 mg/ml
STORAGE: Single dose container.

ADVERSE EFFECTS: Nausea or pain/ redness at the injecton site may occur, Persistent fever, Diarrhoea, drowsiness, Dizziness, Stomach pain, Chest pain, irregular pulse, seizures.

We are one of the leading manufacturers and exporters of mannitol injection of supreme quality.

COMPOSITION:

Each ml contains:

• Mannitol200 mg
• Water for Injectionq.s

DOSAGES: For Intravenous infusion only 200 mg/ml

INDICATIONS: High intraocular pressure when pressure can not be lowered by other means, Urinary excretion of toxic metals , Incresad Intra cranial pressure and brain mass, oliguric phase of acute renel failure before irreversible renal failure becomes established.

ADVERSE EFFECTS: Nausea, Vommiting rhinitis, local pain , skin necrosis, thrombophlebitis at the site of injection, chills, dizziness, utricaria, hypotension, hypertension, tachycardia, fever, angina like chest pain.

Packaging and storage:

Preserve in single-dose glass or plastic containers.

Labeling:

The label states the total osmolar concentration in mOs- mol per L. Where the contents are less than 100 mL, or where the label states that the Injection is not for direct injection but is to be diluted before use, the label alternatively may state the total osmolar concentration in mOsmol per mL. The label also states that it should be warmed before use to dissolve any crystals that may have
formed.

Our range of distilled water is available in a single dose container for intravenous administration after addition of a suitable solute. Also used as a dispensing container for diluent use, any  antimicrobial or other substance is not added in it.
 

• Generic Name: Sterile Water for Injection
• Dosage Form: injection
• USP: Sterile, Non-pyrogenic
• pH:  5.5 (5.0 to 7.0).
• Osmolarity is 0

We use VIAFLEX plastic container that is made from a specially formulated polyvinyl chloride (PL 146 Plastic). The amount permeated from the container into the overwrap is not enough to affect the solution. Only some chemical components may leach out from the plastic container in little amounts, but being safe. It is used in the aseptic preparation of parenteral solutions and as a hemolytic agent due to its hypotonicity. This enables it to be contraindicated for intravenous administration without additives.

We as one of the leading manufacturers in pharmaceutical sector offers saline solution which is in sterile form and is of supreme quality.

COMPOSITION:

Each ml contains

• Sodium chloride 0.9%w/v
• Water for Injection q.s
• CATEGORY: Electrolyte and water
• Fluid and electrolyte replenishment 
• Single dose, sterile, and ready to use vials.
• Daily hygiene for babies and all family members.
  
• Cleanser for nasal cavities especially blocked nose of the babies.
  
• Solution for inhalation by nebulizers.
  
• Eye wash solution

DOSAGE: For Intravenous Infusion only 9 mg/ml
STORAGE: Single dose container

INDICATIONS: Source of water and electrolyte. Priming solution for hemodialysis solutions.

ADVERSE EFFECTS:Fever, infection at the site of injection, venous thrombosis or phlebitis, extravasations, hypervolemia. 

We are one of the leading names in manufacture, export and supply of supreme quality Dexamethasone Injection.

COMPOSITION 

Each ml contains:

• Dexamethasone Sodium Phosphate
• As Dexamethasone Phosphate 4 mg
• Methyl Paraben 0.5%w/v
• Propyl paraben 0.02%w/v
• Water for Injection q.s
• Pack size 2ml vial

Indications:  Allergic reactions ,Pre & post-operatively, Acute state of infections , Poisoning, Adrenocortical insufficiency , Shock Acute dermatological disorders ,Rheumatic disorders Ophthalmologic disorders
 
DOSAGE: 4-20 mg/day IV Infusion or im 0.5-5 mg/day orally

CONTRA-INDICATIONS: Renal failure, Diabetes mellitus, Psychosis, Osteoporosis. Pregnancy. CHF, tuberculosis & other systemic infections  

PRECAUTIONS: May reduce the response of the pituitary-adrenal axis to stress. Glaucoma, epilepsy, Hypertrnsion. Liver dysfunction elderly.

SIDE-EFFECTS: Cushing’s habitus (rounded face , narrow mouth). Fragile skin, easy bruising, telengiectasis, hirsutism. Cutaneous atrophy occurs with topical use. Hyperglycaemia, glycosuria, muscular weakness. Deayed healing of wounds & surgical incisions.

With gentamicin, the vestibular mechanism may be affected when serum level of 10ug / ml is exceeded.  It is used for treatment of:
 

• Bacteraemia
• Post surgical infection
• Septicaemia
• Peritonitis
• Meningitis
• Severe burn and associated infection
• Pneumonia
• Osteomyelitis
• Severe neonatal infections (neonatal )
• Cerebral ventriculitis
• Otitis, prophylaxis
• Treatment of endocarditis due to streptococci
• Urinary tract infection
  

 

Specifications	each 2ml ampoule contains 2ml solution of gentamicin sulphate equivalent to 80mg gentamicin base with preservative
Actions	Synergistic action happens when combined with metronidazole or clindamycin for mixed anaerobic and aerobic infections (separate injections should be used and not to be ), or when combined with ampicillin or benzyl penicillin for enterococci and streptococcal infections (separate injections should be administered and not to be )
Contra indication	for pregnant women and the elder patients: the dosage should be reduced
Elimination	Gentamicin is excreted by simple glomerular filteration
Dosage frequency	Dosage frequency may be predicted by assessing creatinine clearance
Precaution	does not require refrigerated conditions, can be mixed with the following: penicillin, erythromycin, cephalosporin, heparin and sodium bicarbonate

 

We manufacture and export amikacin sulphate injection of high quality.

AMIKACIN SULPHATE INJECTION
SPECIFICATION:

Each ml contains:

• Amikacin Sulphate
• Equivalent to Amikacin 500 mg
• Also contains
• Buffer Agent
• Sodium Citrate 2.5 %w/v
• Preservatives
• Sodium Metabisulphite 0.66%w/v
• Methyl Paraben 0.04%w/v
• Propyl paraben 0.01%w/v
• Sulphuric Acid
• Water for Injection q.s
• AVAILABLE STOCK 100 mg/2 ml, 250 mg/2ml, 500 mg/2 ml
• Pack size 2 ml vial

Indications : Bacteraemias, septicemias, respiratory tract, bone and joints, CNS(including meningitis), soft tissue, intra abdominal infections (including peritonitis), burns and post-operative infections. 

Doasge
IM route for adults,
Children: 15mg/kg body weight/day in 2 or 3 divided doses. Max of 1.5 gm/day.
Neonatals: 10mg/kg body weight followed by 7.5mg/kg every 12 hours IV route dosage is identical, injection spread over 2-3 mins or a slow IV infusion spread over a period of 30+60 mins and for infants and neonatal 1-2 hours.

Contra-Indications
Known hypersensitive to amino glycoside.
Special Precautions: Impaired renal funcation, ensure adequate hydration.