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"70934-920-30" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BOTTLE, PLASTIC (70934-920-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)
NDC Code
70934-920-30
Package Description
30 TABLET in 1 BOTTLE, PLASTIC (70934-920-30)
Product NDC
70934-920
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20211104
End Marketing Date
20240229
Marketing Category Name
ANDA
Application Number
ANDA078925
Manufacturer
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
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/70934-920-30