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"10135-759-90" National Drug Code (NDC)
Amlodipine Besylate 90 TABLET in 1 BOTTLE (10135-759-90)
(Marlex Pharmaceuticals, Inc.)
NDC Code
10135-759-90
Package Description
90 TABLET in 1 BOTTLE (10135-759-90)
Product NDC
10135-759
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20221001
Marketing Category Name
ANDA
Application Number
ANDA207821
Manufacturer
Marlex 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/10135-759-90