Glipizide
- Product NDC
- 16729-139
- 11-digit product format
- 167290139
- Labeler code
- 16729
- Product ID
- 16729-139_ecb57512-ac6b-ad23-e053-2a95a90aacb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Accord Healthcare Inc.
- 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
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16729-139-00 | 16729013900 | 100 TABLET in 1 BOTTLE (16729-139-00) | 100 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |
| 16729-139-16 | 16729013916 | 500 TABLET in 1 BOTTLE (16729-139-16) | 500 tablet | 2011-07-18 | 0000-00-00 | No | No | Current |