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"0172-4358-60" National Drug Code (NDC)
Ranitidine 100 TABLET, FILM COATED in 1 BOTTLE (0172-4358-60)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0172-4358-60
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (0172-4358-60)
Product NDC
0172-4358
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19980401
Marketing Category Name
ANDA
Application Number
ANDA075165
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
300
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/0172-4358-60