Glipizide
- Product NDC
- 68788-9176
- 11-digit product format
- 687889176
- Labeler code
- 68788
- Product ID
- 68788-9176_ec02fb14-1065-4285-bac0-2dbcfe5dd4ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals,Inc.
- Application
- ANDA074305
- Marketing category
- ANDA
- Marketing start
- 2011-04-25
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record