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"49349-381-02" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BLISTER PACK (49349-381-02)
(REMEDYREPACK INC.)
NDC Code
49349-381-02
Package Description
30 TABLET in 1 BLISTER PACK (49349-381-02)
Product NDC
49349-381
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20110822
Marketing Category Name
ANDA
Application Number
ANDA078500
Manufacturer
REMEDYREPACK INC.
Substance Name
AMLODIPINE BESYLATE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-381-02