Tamoxifen Citrate NDC 50090-0485

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-0485Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-0485Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
50090-0485-1	50090048501	60 TABLET in 1 BOTTLE (50090-0485-1)Marketed from Jun 29, 2016

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Route: Oral
Labeler: A-S Medication Solutions
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 070929
Marketing start: Aug 15, 2011
Listing expires: Dec 31, 2027
Other FDA classes: Selective Estrogen Receptor Modulators (Mechanism)
Identifiers: Product ID 50090-0485_b4e41027-4beb-46cc-b12d-38fc3b6f357dSPL ID b4e41027-4beb-46cc-b12d-38fc3b6f357dSPL set ID 8d731e7e-3b04-49a2-a0f6-3779422174ccRxCUI 198240UNII 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

N450090048501 followed by a unit qualifier and the quantity

Package 50090-0485-01. 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 070929

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 070929
Product	Strength	Form · route	Labeler	Product NDC
Tamoxifen Citrate	Tamoxifen citrate 20 mg/1	TabletOral	Proficient Rx LP	63187-976
Tamoxifen Citrate	Tamoxifen citrate 10 mg/1	TabletOral	Actavis Pharma, Inc.	0591-2472
Tamoxifen Citrate	Tamoxifen citrate 20 mg/1	TabletOral	Actavis Pharma, Inc.	0591-2473
Tamoxifen Citrate	Tamoxifen citrate 10 mg/1	TabletOral	Bryant Ranch Prepack	72162-2225
Tamoxifen Citrate	Tamoxifen citrate 20 mg/1	TabletOral	A-S Medication Solutions	50090-0942
Tamoxifen Citrate	Tamoxifen citrate 10 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-5254