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"61919-199-90" National Drug Code (NDC)
Ranitidine Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (61919-199-90)
(Direct Rx)
NDC Code
61919-199-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (61919-199-90)
Product NDC
61919-199
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine Hydrochloride
Non-Proprietary Name
Ranitidine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20171106
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/61919-199-90