Tamoxifen Citrate
NDC 51862-643, Tamoxifen Citrate, tablet, film coated, from Mayne Pharma Commercial LLC.
- Product NDC
- 51862-643
- Status
- Listed
- Labeler
- Mayne Pharma Commercial LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075797
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51862-643 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TAMOXIFEN CITRATE20 mg/1
Pharmacologic classes
Estrogen Agonist/Antagonist [EPC]; Selective Estrogen Receptor Modulators [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51862-643-10 | 51862064310 | 1000 TABLET, FILM COATED in 1 BOTTLE (51862-643-10) |
| 51862-643-30 | 51862064330 | 30 TABLET, FILM COATED in 1 BOTTLE (51862-643-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c82205a3-ae0c-4ce5-b04b-9581cd8c70d4
Use it
Look up 51862-643 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51862-643 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51862-643. 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.