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"49349-025-03" National Drug Code (NDC)
Ranitidine Hydrochloride 20 TABLET in 1 BOTTLE (49349-025-03)
(REMEDYREPACK INC.)
NDC Code
49349-025-03
Package Description
20 TABLET in 1 BOTTLE (49349-025-03)
Product NDC
49349-025
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine Hydrochloride
Non-Proprietary Name
Ranitidine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20131205
Marketing Category Name
ANDA
Application Number
ANDA077824
Manufacturer
REMEDYREPACK INC.
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/49349-025-03