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"68788-1737-1" National Drug Code (NDC)
Amlodipine Besylate 100 TABLET in 1 BOTTLE, PLASTIC (68788-1737-1)
(Preferred Pharmaceuticals, Inc.)
NDC Code
68788-1737-1
Package Description
100 TABLET in 1 BOTTLE, PLASTIC (68788-1737-1)
Product NDC
68788-1737
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
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/68788-1737-1