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"70518-0801-0" National Drug Code (NDC)
Ranitidine 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0801-0)
(REMEDYREPACK INC.)
NDC Code
70518-0801-0
Package Description
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0801-0)
Product NDC
70518-0801
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20171020
Marketing Category Name
ANDA
Application Number
ANDA078542
Manufacturer
REMEDYREPACK INC.
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
150
Strength Unit
mg/1
Pharmacy Classes
Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0801-0