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"61919-381-60" National Drug Code (NDC)
Ranitidine 60 TABLET in 1 BOTTLE (61919-381-60)
(DIRECT RX)
NDC Code
61919-381-60
Package Description
60 TABLET in 1 BOTTLE (61919-381-60)
Product NDC
61919-381
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140101
Marketing Category Name
ANDA
Application Number
ANDA077824
Manufacturer
DIRECT RX
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/61919-381-60