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"61919-713-90" National Drug Code (NDC)
Glipizide 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-713-90)
(Direct_Rx)
NDC Code
61919-713-90
Package Description
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-713-90)
Product NDC
61919-713
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Glipizide
Non-Proprietary Name
Glipizide
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20190819
Marketing Category Name
ANDA
Application Number
ANDA204720
Manufacturer
Direct_Rx
Substance Name
GLIPIZIDE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-713-90