Prescription drug · ANDA
Tamoxifen Citrate NDC 59651-299
Tamoxifen citrate 10 mg/1 · Tablet, Film coated · Oral · Aurobindo Pharma Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 59651-299-60 | 59651029960 | 60 TABLET, FILM COATED in 1 BOTTLE (59651-299-60)Marketed from Aug 14, 2020 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Tamoxifen Citrate
- Generic name (nonproprietary)
- tamoxifen citrate
- Active ingredients
- Tamoxifen citrate — 10 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Aurobindo Pharma Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 213358
- Marketing start
- Listing expires
- Other FDA classes
- Selective Estrogen Receptor Modulators (Mechanism)
- Identifiers
- Product ID 59651-299_a596c715-8e30-43c1-aba3-4fe5de6729faSPL ID a596c715-8e30-43c1-aba3-4fe5de6729faSPL set ID a596c715-8e30-43c1-aba3-4fe5de6729faRxCUI 198240, 313195UNII 7FRV7310N6
- Pharmacologic class
- Estrogen Agonist/Antagonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N459651029960followed by a unit qualifier and the quantityPackage 59651-0299-60. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 213358
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Tamoxifen Citrate | Tamoxifen citrate 10 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals, Inc. | 68071-3990 |
| Tamoxifen Citrate | Tamoxifen citrate 20 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-300 |
| Tamoxifen Citrate | Tamoxifen citrate 10 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2208 |
| Tamoxifen Citrate | Tamoxifen citrate 20 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2209 |