nifedipine
NDC 70807-503, nifedipine, tablet, film coated, extended release, from Elite Pharmaceutical Solution, Inc..
- Product NDC
- 70807-503
- Status
- Listed
- Labeler
- Elite Pharmaceutical Solution, Inc.
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212016
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70807-503 \ -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 |
|---|---|---|
| 70807-503-12 | 70807050312 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70807-503-12) |
| 70807-503-13 | 70807050313 | 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70807-503-13) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/1df07edb-630d-4c70-a68c-bdbc607ce850
Use it
Look up 70807-503 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70807-503 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70807-503. 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.