Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 017033
Company: ABRAXIS PHARM
Company: ABRAXIS PHARM
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
HEPARIN SODIUM | HEPARIN SODIUM | 1,000 UNITS/ML | INJECTABLE;INJECTION | Discontinued | None | No | No |
SODIUM HEPARIN | HEPARIN SODIUM | 5,000 UNITS/ML | INJECTABLE;INJECTION | Discontinued | None | No | No |
SODIUM HEPARIN | HEPARIN SODIUM | 10,000 UNITS/ML | INJECTABLE;INJECTION | Discontinued | None | No | No |
SODIUM HEPARIN | HEPARIN SODIUM | 20,000 UNITS/ML | INJECTABLE;INJECTION | Discontinued | None | No | No |