Glipizide
- Product NDC
- 71335-0039
- 11-digit product format
- 713350039
- Labeler code
- 71335
- Product ID
- 71335-0039_0f25675d-f851-4108-a1e7-3d0819feb6f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074550
- Marketing category
- ANDA
- Marketing start
- 2011-07-18
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0039-1 | 71335003901 | 60 TABLET in 1 BOTTLE (71335-0039-1) | 60 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0039-2 | 71335003902 | 30 TABLET in 1 BOTTLE (71335-0039-2) | 30 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0039-3 | 71335003903 | 100 TABLET in 1 BOTTLE (71335-0039-3) | 100 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0039-4 | 71335003904 | 120 TABLET in 1 BOTTLE (71335-0039-4) | 120 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0039-5 | 71335003905 | 90 TABLET in 1 BOTTLE (71335-0039-5) | 90 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0039-6 | 71335003906 | 20 TABLET in 1 BOTTLE (71335-0039-6) | 20 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0039-7 | 71335003907 | 180 TABLET in 1 BOTTLE (71335-0039-7) | 180 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |