Metoprolol Tartrate
NDC 68071-4769, Metoprolol Tartrate, tablet, film coated, from NuCare Pharmaceuticals,Inc..
- Product NDC
- 68071-4769
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077739
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68071-4769 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METOPROLOL TARTRATE50 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-4769-1 | 68071476901 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-4769-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/81f6854e-72fa-83b9-e053-2a91aa0afe01
Use it
Look up 68071-4769 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-4769 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-4769. 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.