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"59762-7022-1" National Drug Code (NDC)
Glyburide 1000 TABLET in 1 BOTTLE (59762-7022-1)
(Greenstone LLC)
NDC Code
59762-7022-1
Package Description
1000 TABLET in 1 BOTTLE (59762-7022-1)
Product NDC
59762-7022
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Glyburide
Non-Proprietary Name
Glyburide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20071018
End Marketing Date
20140930
Marketing Category Name
ANDA
Application Number
ANDA077537
Manufacturer
Greenstone LLC
Substance Name
GLYBURIDE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59762-7022-1