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
- 72789-463_57ecb215-6656-5aef-e063-6294a90a4539
- Product NDC
- 72789-463
- Form
- TABLET
- Composition / generic term
- Glipizide
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231003
- Source listing expiry
- 20271231
Source-listed ingredients
- GLIPIZIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 360 TABLET in 1 BOTTLE, PLASTIC (72789-463-86) · 72789-463-86
- 90 TABLET in 1 BOTTLE, PLASTIC (72789-463-90) · 72789-463-90
- 180 TABLET in 1 BOTTLE, PLASTIC (72789-463-93) · 72789-463-93
- 1000 TABLET in 1 BOTTLE, PLASTIC (72789-463-95) · 72789-463-95
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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