RANITIDINE HYDROCHLORIDE (RANITIDINE HYDROCHLORIDE) — FDA Approval ANDA211058 (AUROBINDO PHARMA)
RANITIDINE HYDROCHLORIDE (RANITIDINE HYDROCHLORIDE) — FDA Approval ANDA211058 (AUROBINDO PHARMA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: RANITIDINE HYDROCHLORIDE; Active ingredients: RANITIDINE HYDROCHLORIDE; Application number: ANDA211058.
| Brand name | RANITIDINE HYDROCHLORIDE |
|---|---|
| Active ingredients | RANITIDINE HYDROCHLORIDE |
| Application number | ANDA211058 |
| Sponsor | AUROBINDO PHARMA |
| Dosage form | CAPSULE |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 20180716 |
| Source | openFDA Drugs@FDA |
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