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"72789-262-60" National Drug Code (NDC)
Amlodipine Besylate 60 TABLET in 1 BOTTLE, PLASTIC (72789-262-60)
(PD-Rx Pharmaceuticals, Inc.)
NDC Code
72789-262-60
Package Description
60 TABLET in 1 BOTTLE, PLASTIC (72789-262-60)
Product NDC
72789-262
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Proprietary Name Suffix
10 Mg
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20211001
Marketing Category Name
ANDA
Application Number
ANDA078414
Manufacturer
PD-Rx 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/72789-262-60