Tamoxifen Citrate
- Product NDC
- 71335-0662
- 11-digit product format
- 713350662
- Labeler code
- 71335
- Product ID
- 71335-0662_f374f251-1ada-4548-8a7a-7242b8229463
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070929
- Marketing category
- ANDA
- Marketing start
- 2016-07-18
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record