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"52125-971-23" National Drug Code (NDC)
Glipizide 180 TABLET in 1 BOTTLE (52125-971-23)
(REMEDYREPACK INC.)
NDC Code
52125-971-23
Package Description
180 TABLET in 1 BOTTLE (52125-971-23)
Product NDC
52125-971
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Glipizide
Non-Proprietary Name
Glipizide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140616
Marketing Category Name
ANDA
Application Number
ANDA077820
Manufacturer
REMEDYREPACK INC.
Substance Name
GLIPIZIDE
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/52125-971-23