Procardia XL
NDC 0069-2650, nifedipine, tablet, film coated, extended release, from Pfizer Laboratories Div Pfizer Inc.
- Product NDC
- 0069-2650
- Status
- Listed
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA019684
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0069-2650 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NIFEDIPINE30 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0069-2650-41 | 00069265041 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0069-2650-41) |
| 0069-2650-66 | 00069265066 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-66) |
| 0069-2650-72 | 00069265072 | 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-72) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/8ebcb33c-f43b-4b36-9f94-9774b2a59e06
Use it
Look up 0069-2650 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0069-2650 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0069-2650. 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.