Glyburide
- Product NDC
- 55700-725
- 11-digit product format
- 557000725
- Labeler code
- 55700
- Product ID
- 55700-725_d714d65f-df75-427c-9847-b17e96e24669
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA090937
- Marketing category
- ANDA
- Marketing start
- 2019-02-15
- 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
- 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 |
|---|
| 55700-725-30 | 55700072530 | 30 TABLET in 1 BOTTLE (55700-725-30) | 30 tablet | 2019-02-15 | 0000-00-00 | No | No | Current |
| 55700-725-90 | 55700072590 | 90 TABLET in 1 BOTTLE (55700-725-90) | 90 tablet | 2019-02-15 | 0000-00-00 | No | No | Current |