Diltiazem Hydrochloride
NDC 63629-3659, Diltiazem Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 63629-3659
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA074185
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63629-3659 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DILTIAZEM HYDROCHLORIDE30 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A4 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63629-3659-1 | 63629365901 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-3659-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6ca6a648-fc67-4cf8-a1f7-787c9574e3a1
Use it
Look up 63629-3659 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63629-3659 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63629-3659. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.