Glyburide
- Product NDC
- 70518-2695
- 11-digit product format
- 705182695
- Labeler code
- 70518
- Product ID
- 70518-2695_ccfc4a48-4011-ed71-e053-2995a90ac483
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA017532
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-04-16
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2695-0 | 70518269500 | 100 POUCH in 1 BOX (70518-2695-0) > 1 TABLET in 1 POUCH (70518-2695-1) | 100 pouch | 2020-04-16 | 0000-00-00 | No | No | Current |