Glucotrol
- Product NDC
- 0049-4120
- 11-digit product format
- 000494120
- Labeler code
- 0049
- Product ID
- 0049-4120_2caee6e4-a0e9-4a80-9f5e-6591f426f5c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Roerig
- Application
- NDA017783
- Marketing category
- NDA
- Marketing start
- 1984-05-08
- Marketing end
- 2022-01-31
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0049-4120-66 | 00049412066 | 100 TABLET in 1 BOTTLE (0049-4120-66) | 100 tablet | 1984-05-08 | 2022-01-31 | No | No | Current |