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"70518-0389-0" National Drug Code (NDC)
Glipizide 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0389-0)
(REMEDYREPACK INC.)
NDC Code
70518-0389-0
Package Description
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0389-0)
Product NDC
70518-0389
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
20170404
Marketing Category Name
ANDA
Application Number
ANDA076159
Manufacturer
REMEDYREPACK INC.
Substance Name
GLIPIZIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0389-0