Glipizide
- Product NDC
- 63629-6476
- 11-digit product format
- 636296476
- Labeler code
- 63629
- Product ID
- 63629-6476_934ad0e4-069d-4ad1-932a-e02611d96d73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074305
- Marketing category
- ANDA
- Marketing start
- 1995-04-07
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6476-1 | 63629647601 | 90 TABLET in 1 BOTTLE (63629-6476-1) | 90 tablet | 2015-09-09 | 0000-00-00 | No | No | Current |
| 63629-6476-2 | 63629647602 | 30 TABLET in 1 BOTTLE (63629-6476-2) | 30 tablet | 2015-09-09 | 0000-00-00 | No | No | Current |
| 63629-6476-3 | 63629647603 | 60 TABLET in 1 BOTTLE (63629-6476-3) | 60 tablet | 2015-09-09 | 0000-00-00 | No | No | Current |