Tamoxifen Citrate
- Product NDC
- 71335-0237
- 11-digit product format
- 713350237
- Labeler code
- 71335
- Product ID
- 71335-0237_1bb81dd5-8d4e-4d6d-b030-a8ff2a3d4f55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075797
- Marketing category
- ANDA
- Marketing start
- 2016-08-03
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0237-1 | 71335023701 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0237-1) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0237-2 | 71335023702 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0237-2) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0237-3 | 71335023703 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0237-3) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0237-4 | 71335023704 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0237-4) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0237-5 | 71335023705 | 58 TABLET, FILM COATED in 1 BOTTLE (71335-0237-5) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0237-6 | 71335023706 | 52 TABLET, FILM COATED in 1 BOTTLE (71335-0237-6) | 2021-12-27 | 0000-00-00 | No | No | Current |