Tamoxifen Citrate
- Product NDC
- 72162-2209
- 11-digit product format
- 721622209
- Labeler code
- 72162
- Product ID
- 72162-2209_8222e567-8174-40fc-afd8-ab6bde6dc073
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213358
- Marketing category
- ANDA
- Marketing start
- 2020-08-14
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2209-3 | Tamoxifen Citrate | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2209 | TAMOXIFEN CITRATE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20241109_9b4a8abc-6e56-40c5-a826-1d1f3c0786e1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2209-3 | 72162220903 | 30 TABLET, FILM COATED in 1 BOTTLE (72162-2209-3) | 2024-01-05 | No | No | Current |