Pill Identifier Glipizide - NDC 68382-336
Glipizide
Product Code 68382-336
Glipizide by Zydus Pharmaceuticals (usa) Inc. is a orange rou tablet extended release about 6 mm in size, imprinted with 3. The product is a human prescription drug with active ingredient(s) glipizide.
Glipizide
Active Ingredient(s): Glipizide
Inactive Ingredient(s):
- ACETYLTRIBUTYL CITRATE
- AMMONIA
- BUTYL ALCOHOL
- FD&C YELLOW NO. 6
- FERROSOFERRIC OXIDE
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED
- HYPROMELLOSES
- ISOPROPYL ALCOHOL
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- POLYETHYLENE GLYCOLS
- PROPYLENE GLYCOL
- SHELLAC
- SILICON DIOXIDE
- TITANIUM DIOXIDE
Zydus Pharmaceuticals (usa) Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Extended Release
- Orange (C48331)
Product Packages
NDC Package Code | Package Description |
---|---|
68382-336-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE |
68382-336-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE |
68382-336-06 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE |
68382-336-10 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE |
68382-336-14 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE |
68382-336-16 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE |
68382-336-77 | 10 BLISTER PACK in 1 CARTON > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68382-336-30) |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.