Glipizide
- Product NDC
- 63629-1394
- 11-digit product format
- 636291394
- Labeler code
- 63629
- Product ID
- 63629-1394_2fa39150-8fd7-4d10-9ff8-f6e9f7407018
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074223
- Marketing category
- ANDA
- Marketing start
- 1995-02-27
- 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
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 |
|---|
| 63629-1394-1 | 63629139401 | 60 TABLET in 1 BOTTLE (63629-1394-1) | 60 tablet | 2004-12-07 | 0000-00-00 | No | No | Current |
| 63629-1394-2 | 63629139402 | 30 TABLET in 1 BOTTLE (63629-1394-2) | 30 tablet | 2004-12-07 | 0000-00-00 | No | No | Current |
| 63629-1394-3 | 63629139403 | 100 TABLET in 1 BOTTLE (63629-1394-3) | 100 tablet | 2004-12-24 | 0000-00-00 | No | No | Current |
| 63629-1394-4 | 63629139404 | 120 TABLET in 1 BOTTLE (63629-1394-4) | 120 tablet | 2012-01-18 | 0000-00-00 | No | No | Current |
| 63629-1394-5 | 63629139405 | 90 TABLET in 1 BOTTLE (63629-1394-5) | 90 tablet | 2011-06-23 | 0000-00-00 | No | No | Current |
| 63629-1394-6 | 63629139406 | 20 TABLET in 1 BOTTLE (63629-1394-6) | 20 tablet | 2011-09-21 | 0000-00-00 | No | No | Current |
| 63629-1394-7 | 63629139407 | 180 TABLET in 1 BOTTLE (63629-1394-7) | 180 tablet | 2014-05-14 | 0000-00-00 | No | No | Current |