FDA NDC Directory · JSON-LD · Markdown
NDC 70247-012 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE
| Generic name | Duloxetine |
|---|---|
| Labeler / Manufacturer | Qingdao BAHEAL Pharmaceutical Co., Ltd. |
| Marketing category | Abbreviated NDA (generic) · App ANDA210599 |
| Dosage form / route | CAPSULE, DELAYED RELEASE · ORAL |
| Active ingredients | DULOXETINE HYDROCHLORIDE (20 mg/1) |
| Marketing started | 20180505 |
| Package count | 1 |
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