Tamoxifen Citrate
- Product NDC
- 0179-0224
- 11-digit product format
- 001790224
- Labeler code
- 0179
- Product ID
- 0179-0224_7c4ead10-374a-70e2-e053-2a91aa0afebc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA075797
- Marketing category
- ANDA
- Marketing start
- 2017-01-12
- Marketing end
- 2020-02-29
- Substance
- TAMOXIFEN CITRATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record