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"70934-075-30" National Drug Code (NDC)

Amlodipine Besylate 30 TABLET in 1 BOTTLE, PLASTIC (70934-075-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-075-30
Package Description30 TABLET in 1 BOTTLE, PLASTIC (70934-075-30)
Product NDC70934-075
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180202
End Marketing Date20250131
Marketing Category NameANDA
Application NumberANDA078925
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium 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/70934-075-30





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