Glyburide
- Product NDC
- 55289-606
- 11-digit product format
- 552890606
- Labeler code
- 55289
- Product ID
- 55289-606_da322850-5a20-3c63-e053-2995a90ad78f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA017532
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1984-05-01
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 3 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55289-606-30 | 55289060630 | 30 TABLET in 1 BOTTLE, PLASTIC (55289-606-30) | 30 tablet | 2016-01-27 | 0000-00-00 | No | No | Current |