Glipizide
- Product NDC
- 71335-0036
- 11-digit product format
- 713350036
- Labeler code
- 71335
- Product ID
- 71335-0036_464f4284-556f-432f-9f9f-b1dff3520358
- 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
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0036-1 | 71335003601 | 100 TABLET in 1 BOTTLE (71335-0036-1) | 100 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0036-2 | 71335003602 | 30 TABLET in 1 BOTTLE (71335-0036-2) | 30 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0036-3 | 71335003603 | 60 TABLET in 1 BOTTLE (71335-0036-3) | 60 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0036-4 | 71335003604 | 90 TABLET in 1 BOTTLE (71335-0036-4) | 90 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0036-5 | 71335003605 | 20 TABLET in 1 BOTTLE (71335-0036-5) | 20 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0036-6 | 71335003606 | 180 TABLET in 1 BOTTLE (71335-0036-6) | 180 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 71335-0036-7 | 71335003607 | 10 TABLET in 1 BOTTLE (71335-0036-7) | 10 tablet | 2014-01-16 | 0000-00-00 | No | No | Current |