Tamoxifen Citrate
- Product NDC
- 50090-0942
- 11-digit product format
- 500900942
- Labeler code
- 50090
- Product ID
- 50090-0942_7bfc1a17-2123-4f1b-bde7-cd6763ec10da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070929
- Marketing category
- ANDA
- Marketing start
- 2011-08-15
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tamoxifen Citrate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TAMOXIFEN CITRATE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7FRV7310N6 |
| Rxcui | 313195 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-0942-0 | Tamoxifen Citrate | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0942 | TAMOXIFEN CITRATE TABLET [A-S MEDICATION SOLUTIONS] | 14 | Current NDC, Legacy NDC, 1 package rows | 20240113_716657e8-d809-4671-87bc-8d10ef69a071.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0942-0 | 50090094200 | 90 TABLET in 1 BOTTLE, PLASTIC (50090-0942-0) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |