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"68788-6386-9" National Drug Code (NDC)
Amlodipine Besylate 90 TABLET in 1 BOTTLE (68788-6386-9)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-6386-9
Package Description
90 TABLET in 1 BOTTLE (68788-6386-9)
Product NDC
68788-6386
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160504
Marketing Category Name
ANDA
Application Number
ANDA077073
Manufacturer
Preferred Pharmaceuticals Inc.
Substance Name
AMLODIPINE BESYLATE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-6386-9