Tamoxifen Citrate
- Product NDC
- 51407-439
- 11-digit product format
- 514070439
- Labeler code
- 51407
- Product ID
- 51407-439_dd8217d4-a044-a596-e053-2995a90a3593
- 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
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-439 | TAMOXIFEN CITRATE TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.] | 6 | Legacy NDC | 20241213_cadef490-5dc6-7230-e053-2a95a90a5551.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-439-60 | 51407043960 | 60 TABLET, FILM COATED in 1 BOTTLE (51407-439-60) | 2021-08-02 | 0000-00-00 | No | No | Current |