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"42708-008-30" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BOTTLE (42708-008-30)
(QPharma Inc)
NDC Code
42708-008-30
Package Description
30 TABLET in 1 BOTTLE (42708-008-30)
Product NDC
42708-008
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20070710
Marketing Category Name
ANDA
Application Number
ANDA076846
Manufacturer
QPharma 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/42708-008-30