RANITIDINE HYDROCHLORIDE (RANITIDINE HYDROCHLORIDE) — FDA Approval ANDA078890 (LANNETT CO INC)
RANITIDINE HYDROCHLORIDE (RANITIDINE HYDROCHLORIDE) — FDA Approval ANDA078890 (LANNETT CO INC) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: RANITIDINE HYDROCHLORIDE; Active ingredients: RANITIDINE HYDROCHLORIDE; Application number: ANDA078890.
| Brand name | RANITIDINE HYDROCHLORIDE |
|---|---|
| Active ingredients | RANITIDINE HYDROCHLORIDE |
| Application number | ANDA078890 |
| Sponsor | LANNETT CO INC |
| Dosage form | SYRUP |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 20100701 |
| Source | openFDA Drugs@FDA |
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