United States · FDA National Drug Code directory
Alprazolam
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69339-201_885d0fec-f1a6-42f4-8617-1d048cb15ee9
- Product NDC
- 69339-201
- Form
- TABLET
- Composition / generic term
- Alprazolam
- Labeler
- Natco Pharma USA LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230728
- Source listing expiry
- 20271231
Source-listed ingredients
- ALPRAZOLAM — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (69339-201-01) · 69339-201-01
- 500 TABLET in 1 BOTTLE (69339-201-05) · 69339-201-05
- 1000 TABLET in 1 BOTTLE (69339-201-10) · 69339-201-10
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →