Glyburide
- Product NDC
- 63629-6840
- 11-digit product format
- 636296840
- Labeler code
- 63629
- Product ID
- 63629-6840_607656ac-50d5-401e-97b7-b0e7b86ee45d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLYBURIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090937
- Marketing category
- ANDA
- Marketing start
- 2010-10-05
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 5 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
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 |
|---|
| 63629-6840-1 | 63629684001 | 30 TABLET in 1 BOTTLE (63629-6840-1) | 30 tablet | 2015-11-03 | 0000-00-00 | No | No | Current |