Alprazolam NDC 71335-2133

Product information

Brand name (proprietary)

Alprazolam

Generic name (nonproprietary)

alprazolam

Active ingredients

Alprazolam — .25 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 074342

Marketing start

Oct 1, 1993

Listing expires

Dec 31, 2026

DEA schedule

CIV

Other FDA classes

Benzodiazepines (Chemical structure)

Identifiers

Product ID 71335-2133_8ea1648d-8205-4d5f-af0c-b77772d049dbSPL ID 8ea1648d-8205-4d5f-af0c-b77772d049dbSPL set ID 8ca8e0fc-6c3d-48d4-ad04-708182b45350RxCUI 308047UNII 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

N471335213300 followed by a unit qualifier and the quantity Copy

Package 71335-2133-00. 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.