← FDA Drug Approvals (Drugs@FDA)
DEXTROSE 5% AND ELECTROLYTE NO. 48 IN PLASTIC CONTAINER
NDA · New Drug Application · Sponsor: BAXTER HLTHCARE · Approved 1979-02-02
Drug application
- FDA Application #
NDA017484- Application type
- New Drug Application
- Brand name
- DEXTROSE 5% AND ELECTROLYTE NO. 48 IN PLASTIC CONTAINER
- Generic name
- SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, MONOBASIC POTASSIUM PHOSPHATE, SODIUM CHLORIDE AND DEXTROSE MONOHYDRATE
- Active ingredients
- DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM LACTATE
- Dosage form
- INJECTABLE
- Route
- INJECTION
- Marketing status
- Prescription
- Sponsor
- BAXTER HLTHCARE
- Manufacturer
- Baxter Healthcare Company
- First approval
- 1979-02-02
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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