glyburide and metformin hydrochloride
- Product NDC
- 55700-469
- 11-digit product format
- 557000469
- Labeler code
- 55700
- Product ID
- 55700-469_4b2fe109-f668-493f-8499-64dde41904d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glyburide and metformin hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA206748
- Marketing category
- ANDA
- Marketing start
- 2016-04-07
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 3 mg/1; mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record