Glipizide
- Product NDC
- 63629-2203
- 11-digit product format
- 636292203
- Labeler code
- 63629
- Product ID
- 63629-2203_2660d19a-c0d5-4e9e-8a52-17c323fa1f78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076159
- Marketing category
- ANDA
- Marketing start
- 2016-12-21
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-2203-1 | 63629220301 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2203-1) | 2021-05-19 | 0000-00-00 | No | No | Current |