Tamoxifen Citrate
- Product NDC
- 72162-2208
- 11-digit product format
- 721622208
- Labeler code
- 72162
- Product ID
- 72162-2208_681529be-51fc-4ac3-902a-2e00beb327a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213358
- Marketing category
- ANDA
- Marketing start
- 2020-08-14
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7FRV7310N6 | TAMOXIFEN CITRATE | 54965-24-1 | TAMOXIFEN CITRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2208-6 | 72162220806 | 60 TABLET, FILM COATED in 1 BOTTLE (72162-2208-6) | 2024-01-05 | No | No | Historical |