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"61786-214-02" National Drug Code (NDC)
Ranitidine 1 BOTTLE in 1 CARTON (61786-214-02) > 30 TABLET, FILM COATED in 1 BOTTLE
(REMEDYREPACK INC.)
NDC Code
61786-214-02
Package Description
1 BOTTLE in 1 CARTON (61786-214-02) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC
61786-214
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20150309
Marketing Category Name
ANDA
Application Number
ANDA201745
Manufacturer
REMEDYREPACK INC.
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
75
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/61786-214-02