Metoprolol Tartrate
NDC 71610-137, Metoprolol Tartrate, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-137
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- 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/71610-137 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METOPROLOL TARTRATE25 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71610-137-60 | 71610013760 | 90 TABLET, FILM COATED in 1 BOTTLE (71610-137-60) |
| 71610-137-80 | 71610013780 | 180 TABLET, FILM COATED in 1 BOTTLE (71610-137-80) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b60d2cb0-f2c3-4ad5-8060-5179d5b94256
Use it
Look up 71610-137 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-137 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-137. 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.