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"51655-869-52" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BOTTLE, PLASTIC (51655-869-52)
(Northwind Pharmaceuticals, LLC)
NDC Code
51655-869-52
Package Description
30 TABLET in 1 BOTTLE, PLASTIC (51655-869-52)
Product NDC
51655-869
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230825
Marketing Category Name
ANDA
Application Number
ANDA077073
Manufacturer
Northwind Pharmaceuticals, LLC
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/51655-869-52