United States · FDA National Drug Code directory
Glipizide
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
- 71335-2528_a619f719-a861-4850-8570-7bba46bf7527
- Product NDC
- 71335-2528
- Form
- TABLET
- Composition / generic term
- Glipizide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231003
- Source listing expiry
- 20271231
Source-listed ingredients
- GLIPIZIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (71335-2528-1) · 71335-2528-1
- 30 TABLET in 1 BOTTLE (71335-2528-2) · 71335-2528-2
- 60 TABLET in 1 BOTTLE (71335-2528-3) · 71335-2528-3
- 90 TABLET in 1 BOTTLE (71335-2528-4) · 71335-2528-4
- 20 TABLET in 1 BOTTLE (71335-2528-5) · 71335-2528-5
- 180 TABLET in 1 BOTTLE (71335-2528-6) · 71335-2528-6
- 10 TABLET in 1 BOTTLE (71335-2528-7) · 71335-2528-7
Source and coverage
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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.
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