Glynase
- Product NDC
- 0009-0352
- 11-digit product format
- 000090352
- Labeler code
- 0009
- Product ID
- 0009-0352_03bce5d4-2e0d-41c5-8048-ceb4749b0b5a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Pharmacia and Upjohn Company LLC
- Application
- NDA020051
- Marketing category
- NDA
- Marketing start
- 1992-03-04
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 3 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 |
|---|
| 0009-0352-01 | 00009035201 | 100 TABLET in 1 BOTTLE, PLASTIC (0009-0352-01) | 100 tablet | 1992-03-04 | 0000-00-00 | No | No | Current |
| 0009-0352-04 | 00009035204 | 1000 TABLET in 1 BOTTLE, PLASTIC (0009-0352-04) | 1000 tablet | 1992-03-04 | 0000-00-00 | No | No | Current |