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"0603-2110-60" National Drug Code (NDC)
Amlodipine Besylate 45 TABLET in 1 BOTTLE, PLASTIC (0603-2110-60)
(Par Pharmaceutical)
NDC Code
0603-2110-60
Package Description
45 TABLET in 1 BOTTLE, PLASTIC (0603-2110-60)
Product NDC
0603-2110
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20100407
End Marketing Date
20190531
Marketing Category Name
ANDA
Application Number
ANDA078414
Manufacturer
Par Pharmaceutical
Substance Name
AMLODIPINE BESYLATE
Strength
10
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/0603-2110-60