NDC 68382-185 – Glipizide and Metformin Hydrochloride
Glipizide 2.5 mg/1; Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-185
Product details
- Brand name
- Glipizide and Metformin Hydrochloride
- Generic name
- Glipizide and Metformin Hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078905
- Marketed since
- May 5, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide; Sulfonylurea
Active ingredients
- Glipizide 2.5 mg/1
- Metformin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Glipizide and Metformin Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68382-185-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-185-01) | May 5, 2016 |
| 68382-185-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-185-10) | May 5, 2016 |
| 68382-185-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-185-16) | May 5, 2016 |
| 68382-185-77 | 10 BLISTER PACK in 1 CARTON (68382-185-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-185-30) | May 5, 2016 |
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