Glipizide
- Product NDC
- 63629-8181
- 11-digit product format
- 636298181
- Labeler code
- 63629
- Product ID
- 63629-8181_da2b33e3-0444-4301-b46f-6b304d18b3be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204720
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8181-1 | 63629818101 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-8181-1) | 2019-07-25 | 0000-00-00 | No | No | Current |