Nifedipine
NDC 72789-486, Nifedipine, tablet, extended release, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 72789-486
- Status
- Listed
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216067
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72789-486 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NIFEDIPINE90 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72789-486-01 | 72789048601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-486-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/8e5e126a-7da6-4ceb-b72b-5c9dcc7d7769
Use it
Look up 72789-486 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72789-486 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72789-486. 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.