Glipizide
- Product NDC
- 70518-2549
- 11-digit product format
- 705182549
- Labeler code
- 70518
- Product ID
- 70518-2549_b3263735-d58e-18e7-e053-2995a90abf1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076467
- Marketing category
- ANDA
- Marketing start
- 2020-01-20
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record