Glipizide
- Product NDC
- 71335-0851
- 11-digit product format
- 713350851
- Labeler code
- 71335
- Product ID
- 71335-0851_4f6fa5a3-6c43-40d9-84f5-5b63f26582bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076159
- Marketing category
- ANDA
- Marketing start
- 2016-12-21
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0851-1 | 71335085101 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0851-1) | 2018-06-11 | 0000-00-00 | No | No | Current |
| 71335-0851-2 | 71335085102 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0851-2) | 2018-06-11 | 0000-00-00 | No | No | Current |
| 71335-0851-3 | 71335085103 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0851-3) | 2018-06-11 | 0000-00-00 | No | No | Current |
| 71335-0851-4 | 71335085104 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0851-4) | 2018-06-11 | 0000-00-00 | No | No | Current |
| 71335-0851-5 | 71335085105 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0851-5) | 2018-06-11 | 0000-00-00 | No | No | Current |