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"49349-165-02" National Drug Code (NDC)
Ranitidine Hydrochloride 30 TABLET in 1 BLISTER PACK (49349-165-02)
(REMEDYREPACK INC.)
NDC Code
49349-165-02
Package Description
30 TABLET in 1 BLISTER PACK (49349-165-02)
Product NDC
49349-165
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine Hydrochloride
Non-Proprietary Name
Ranitidine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20110414
Marketing Category Name
ANDA
Application Number
ANDA074680
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/49349-165-02