FDA NDC Directory · JSON-LD · Markdown
NDC 70771-1038 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE
| Generic name | diltiazem hydrochloride |
|---|---|
| Labeler / Manufacturer | Zydus Lifesciences Limited |
| Marketing category | Abbreviated NDA (generic) · App ANDA206641 |
| Dosage form / route | CAPSULE, EXTENDED RELEASE · ORAL |
| Active ingredients | DILTIAZEM HYDROCHLORIDE (300 mg/1) |
| Marketing started | 20171108 |
| Package count | 5 |
Source: openFDA. Public-domain (CC0).