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"68180-751-17" National Drug Code (NDC)
Amlodipine Besylate 300 TABLET in 1 BOTTLE (68180-751-17)
(Lupin Pharmaceuticals, Inc.)
NDC Code
68180-751-17
Package Description
300 TABLET in 1 BOTTLE (68180-751-17)
Product NDC
68180-751
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20070803
End Marketing Date
20210731
Marketing Category Name
ANDA
Application Number
ANDA078043
Manufacturer
Lupin Pharmaceuticals, Inc.
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/68180-751-17