Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 070031
Company: ABRAXIS PHARM
Company: ABRAXIS PHARM
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
SODIUM NITROPRUSSIDE | SODIUM NITROPRUSSIDE | 50MG/VIAL | INJECTABLE;INJECTION | Discontinued | None | No | No |