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"10135-759-10" National Drug Code (NDC)

Amlodipine Besylate 1000 TABLET in 1 BOTTLE (10135-759-10)
(Marlex Pharmaceuticals, Inc.)

NDC Code10135-759-10
Package Description1000 TABLET in 1 BOTTLE (10135-759-10)
Product NDC10135-759
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20221001
Marketing Category NameANDA
Application NumberANDA207821
ManufacturerMarlex Pharmaceuticals, Inc.
Substance NameAMLODIPINE BESYLATE
Strength2.5
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/10135-759-10





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