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"70518-2888-1" National Drug Code (NDC)
Glipizide 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2888-1)
(REMEDYREPACK INC.)
NDC Code
70518-2888-1
Package Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2888-1)
Product NDC
70518-2888
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Glipizide
Non-Proprietary Name
Glipizide
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20200915
Marketing Category Name
ANDA
Application Number
ANDA206928
Manufacturer
REMEDYREPACK INC.
Substance Name
GLIPIZIDE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2888-1