NDC 71335-1042 – Glipizide
Glipizide 2.5 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71335-1042
Product details
- Brand name
- Glipizide
- Generic name
- Glipizide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204720
- Marketed since
- April 24, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Sulfonylurea
Active ingredients
- Glipizide 2.5 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1042-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1042-1) | Jan 8, 2019 |
| 71335-1042-2 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1042-2) | Jan 8, 2019 |
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