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
- 60505-0141_bac5c69c-3714-aa20-b889-dad244e07b9e
- Product NDC
- 60505-0141
- Form
- TABLET
- Composition / generic term
- Glipizide
- Labeler
- Apotex Corp.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020925
- 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 (60505-0141-0) · 60505-0141-0
- 1000 TABLET in 1 BOTTLE (60505-0141-1) · 60505-0141-1
- 500 TABLET in 1 BOTTLE (60505-0141-2) · 60505-0141-2
- 18000 TABLET in 1 BOTTLE (60505-0141-8) · 60505-0141-8
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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