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"57664-055-99" National Drug Code (NDC)
Amlodipine Besylate 90 TABLET in 1 BOTTLE (57664-055-99)
(Caraco Pharmaceutical Laboratories, Ltd.)
NDC Code
57664-055-99
Package Description
90 TABLET in 1 BOTTLE (57664-055-99)
Product NDC
57664-055
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20121019
Marketing Category Name
ANDA
Application Number
ANDA078552
Manufacturer
Caraco Pharmaceutical Laboratories, Ltd.
Substance Name
AMLODIPINE BESYLATE
Strength
2.5
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-055-99