Tamoxifen Citrate
- Product NDC
- 71335-0893
- 11-digit product format
- 713350893
- Labeler code
- 71335
- Product ID
- 71335-0893_a4a8d2bc-8324-47a3-985b-114448547c7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074732
- Marketing category
- ANDA
- Marketing start
- 2003-02-20
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0893-1 | 71335089301 | 30 TABLET in 1 BOTTLE (71335-0893-1) | 30 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |
| 71335-0893-2 | 71335089302 | 60 TABLET in 1 BOTTLE (71335-0893-2) | 60 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |
| 71335-0893-3 | 71335089303 | 90 TABLET in 1 BOTTLE (71335-0893-3) | 90 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |
| 71335-0893-4 | 71335089304 | 28 TABLET in 1 BOTTLE (71335-0893-4) | 28 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |
| 71335-0893-5 | 71335089305 | 58 TABLET in 1 BOTTLE (71335-0893-5) | 58 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |
| 71335-0893-6 | 71335089306 | 52 TABLET in 1 BOTTLE (71335-0893-6) | 52 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |