Tamoxifen Citrate
- Product NDC
- 70518-1881
- 11-digit product format
- 705181881
- Labeler code
- 70518
- Product ID
- 70518-1881_825bddfa-b27d-4e7c-e053-2a91aa0a1deb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070929
- Marketing category
- ANDA
- Marketing start
- 2019-02-19
- Marketing end
- 0000-00-00
- Substance
- TAMOXIFEN CITRATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record