Glipizide
- Product NDC
- 63629-9281
- 11-digit product format
- 636299281
- Labeler code
- 63629
- Product ID
- 63629-9281_4b720506-312e-40f7-9d57-815bf85e104d
- 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
- 5 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 |
|---|
| 63629-9281-1 | 63629928101 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9281-1) | 2022-06-06 | 0000-00-00 | No | No | Current |