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"61786-056-15" National Drug Code (NDC)
Ranitidine Hydrochloride 15 TABLET, FILM COATED in 1 BOTTLE (61786-056-15)
(REMEDYREPACK INC.)
NDC Code
61786-056-15
Package Description
15 TABLET, FILM COATED in 1 BOTTLE (61786-056-15)
Product NDC
61786-056
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
20141013
Marketing Category Name
ANDA
Application Number
ANDA074467
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/61786-056-15