Glyburide

Product NDC
49999-113
11-digit product format
499990113
Labeler code
49999
Product ID
49999-113_04c549eb-07cb-416f-a0d9-9efd2c7eb012
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glyburide
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA074388
Marketing category
ANDA
Marketing start
2011-02-23
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
2019-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
SX6K58TVWCGLYBURIDE10238-21-8GLYBURIDE