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
- 61442-115_2386d706-9dab-4ae0-e063-6394a90a8a06
- Product NDC
- 61442-115
- Form
- TABLET
- Composition / generic term
- Glimepiride
- Labeler
- Carlsbad Technology, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120101
- Source listing expiry
- 20261231
Source-listed ingredients
- GLIMEPIRIDE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (61442-115-01) · 61442-115-01
- 500 TABLET in 1 BOTTLE (61442-115-05) · 61442-115-05
- 1000 TABLET in 1 BOTTLE (61442-115-10) · 61442-115-10
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 →