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"68788-1738-1" National Drug Code (NDC)
Amlodipine Besylate 100 TABLET in 1 BOTTLE (68788-1738-1)
(Preferred Pharmaceuticals, Inc.)
NDC Code
68788-1738-1
Package Description
100 TABLET in 1 BOTTLE (68788-1738-1)
Product NDC
68788-1738
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20100407
Marketing Category Name
ANDA
Application Number
ANDA078414
Manufacturer
Preferred 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/68788-1738-1