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"57664-056-18" National Drug Code (NDC)
Amlodipine Besylate 1000 TABLET in 1 BOTTLE (57664-056-18)
(Caraco Pharmaceutical Laboratories, Ltd.)
NDC Code
57664-056-18
Package Description
1000 TABLET in 1 BOTTLE (57664-056-18)
Product NDC
57664-056
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
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/57664-056-18