Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 086765
Company: NOVARTIS
Company: NOVARTIS
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
IMIPRAMINE HYDROCHLORIDE | IMIPRAMINE HYDROCHLORIDE | 25MG/ML | CONCENTRATE;ORAL | Discontinued | None | No | No |