United States · FDA National Drug Code directory

Glimepiride

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: 43063-698_2b376d88-25a8-b97f-e063-6394a90adfed
Product NDC: 43063-698
Form: TABLET
Composition / generic term: Glimepiride
Labeler: PD-Rx Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20120101
Source listing expiry: 20261231

Source-listed ingredients

GLIMEPIRIDE — 2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE, PLASTIC (43063-698-30) · 43063-698-30
90 TABLET in 1 BOTTLE, PLASTIC (43063-698-90) · 43063-698-90
180 TABLET in 1 BOTTLE, PLASTIC (43063-698-93) · 43063-698-93

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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