Tamoxifen Citrate
- Product NDC
- 60429-910
- 11-digit product format
- 604290910
- Labeler code
- 60429
- Product ID
- 60429-910_ebcca924-03a3-277b-e053-2a95a90a429f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA075797
- Marketing category
- ANDA
- Marketing start
- 2003-02-20
- Marketing end
- 2023-02-28
- 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
- 0000-00-00
- 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 |
|---|
| 60429-910-30 | 60429091030 | 30 TABLET, FILM COATED in 1 BOTTLE (60429-910-30) | 2016-09-28 | 0000-00-00 | No | No | Current |