Glipizide
- Product NDC
- 63629-5256
- 11-digit product format
- 636295256
- Labeler code
- 63629
- Product ID
- 63629-5256_02b6b0e9-1796-4460-a7a2-017c36fd46a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076467
- Marketing category
- ANDA
- Marketing start
- 2006-04-03
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 3 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-5256-1 | 63629525601 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-5256-1) | 2014-03-04 | 0000-00-00 | No | No | Current |
| 63629-5256-2 | 63629525602 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-5256-2) | 2022-02-08 | 0000-00-00 | No | No | Current |
| 63629-5256-3 | 63629525603 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-5256-3) | 2022-02-08 | 0000-00-00 | No | No | Current |