FDA NDC Directory · JSON-LD · Markdown
NDC 52544-693 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE
| Generic name | Diltiazem Hydrochloride |
|---|---|
| Labeler / Manufacturer | Actavis Pharma, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA077686 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | DILTIAZEM HYDROCHLORIDE (300 mg/1) |
| Marketing started | 20110328 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).