RANITIDINE HYDROCHLORIDE (RANITIDINE HYDROCHLORIDE) — FDA Approval ANDA075439 (SUN PHARM INDS LTD)
RANITIDINE HYDROCHLORIDE (RANITIDINE HYDROCHLORIDE) — FDA Approval ANDA075439 (SUN PHARM INDS LTD) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: RANITIDINE HYDROCHLORIDE; Active ingredients: RANITIDINE HYDROCHLORIDE; Application number: ANDA075439.
| Brand name | RANITIDINE HYDROCHLORIDE |
|---|---|
| Active ingredients | RANITIDINE HYDROCHLORIDE |
| Application number | ANDA075439 |
| Sponsor | SUN PHARM INDS LTD |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 20000419 |
| Source | openFDA Drugs@FDA |
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