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"68788-8263-1" National Drug Code (NDC)
Amlodipine Besylate 100 TABLET in 1 BOTTLE (68788-8263-1)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-8263-1
Package Description
100 TABLET in 1 BOTTLE (68788-8263-1)
Product NDC
68788-8263
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20220919
Marketing Category Name
ANDA
Application Number
ANDA078925
Manufacturer
Preferred Pharmaceuticals Inc.
Substance Name
AMLODIPINE BESYLATE
Strength
2.5
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/68788-8263-1