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"61786-381-19" National Drug Code (NDC)
Ranitidine 90 TABLET in 1 BOTTLE (61786-381-19)
(REMEDYREPACK INC.)
NDC Code
61786-381-19
Package Description
90 TABLET in 1 BOTTLE (61786-381-19)
Product NDC
61786-381
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160311
Marketing Category Name
ANDA
Application Number
ANDA077824
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/61786-381-19