← FDA Drug Approvals (Drugs@FDA)
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45%
NDA · New Drug Application · Sponsor: FRESENIUS KABI USA · Approved 1972-02-22
Drug application
- FDA Application #
NDA017029- Application type
- New Drug Application
- Brand name
- HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45%
- Generic name
- HEPARIN SODIUM
- Active ingredients
- HEPARIN SODIUM
- Dosage form
- INJECTABLE
- Route
- INJECTION
- Marketing status
- Prescription
- Sponsor
- FRESENIUS KABI USA
- Manufacturer
- Fresenius Kabi USA, LLC
- First approval
- 1972-02-22
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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