NDC 71335-0967 – Glyburide and Metformin Hydrochloride
Glyburide 5 mg/1; Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0967
Product details
- Brand name
- Glyburide and Metformin Hydrochloride
- Generic name
- Glyburide and Metformin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077870
- Marketed since
- November 14, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide; Sulfonylurea
Active ingredients
- Glyburide 5 mg/1
- Metformin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Glyburide and Metformin Hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0967-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0967-1) | Oct 15, 2018 |
| 71335-0967-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0967-3) | Oct 15, 2018 |
| 71335-0967-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0967-4) | May 30, 2024 |
| 71335-0967-5 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0967-5) | May 30, 2024 |
| 71335-0967-6 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0967-6) | Oct 11, 2018 |
| 71335-0967-7 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0967-7) | May 30, 2024 |
| 71335-0967-8 | 25 TABLET, FILM COATED in 1 BOTTLE (71335-0967-8) | May 30, 2024 |
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