Alprazolam NDC 0228-2039

NDC codes

FDA NDC Directory

Product NDC (as listed)0228-2039Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00228-2039Add 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
0228-2039-10	00228203910	100 TABLET in 1 BOTTLE (0228-2039-10)Marketed from Oct 1, 1993

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Alprazolam
Generic name (nonproprietary): alprazolam
Active ingredients: Alprazolam — 2 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Actavis Pharma, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074342
Marketing start: Oct 1, 1993
Listing expires: Dec 31, 2027
DEA schedule: CIV
Other FDA classes: Benzodiazepines (Chemical structure)
Identifiers: Product ID 0228-2039_08d09d46-386d-4dc8-a0c1-5711261c6282SPL ID 08d09d46-386d-4dc8-a0c1-5711261c6282SPL set ID a23063c0-099a-4256-b95f-3a857bbf704bRxCUI 197321, 197322, 308047, 308048UNII YU55MQ3IZY
Pharmacologic class: Benzodiazepine

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

N400228203910 followed by a unit qualifier and the quantity

Package 00228-2039-10. 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 074342

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

FDA NDC Directory listings under ANDA 074342
Product	Strength	Form · route	Labeler	Product NDC
Alprazolam	Alprazolam .5 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-313
Alprazolam	Alprazolam .5 mg/1	TabletOral	Actavis Pharma, Inc.	0228-2029
Alprazolam	Alprazolam 1 mg/1	TabletOral	Actavis Pharma, Inc.	0228-2031
Alprazolam	Alprazolam 1 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-328
Alprazolam	Alprazolam .25 mg/1	TabletOral	Bryant Ranch Prepack	71335-2133
Alprazolam	Alprazolam .25 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-112
Alprazolam	Alprazolam 1 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-113
Alprazolam	Alprazolam .25 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-2292
Alprazolam	Alprazolam .5 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-2220
Alprazolam	Alprazolam .5 mg/1	TabletOral	A-S Medication Solutions	50090-5078
Alprazolam	Alprazolam .5 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0099
Alprazolam	Alprazolam 1 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0110
Alprazolam	Alprazolam .5 mg/1	TabletOral	Bryant Ranch Prepack	71335-0849
Alprazolam	Alprazolam .25 mg/1	TabletOral	Actavis Pharma, Inc.	0228-2027