www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"59762-2135-9" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (59762-2135-9)
(Greenstone LLC)

NDC Code59762-2135-9
Package Description90 TABLET in 1 BOTTLE (59762-2135-9)
Product NDC59762-2135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20190624
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA019787
ManufacturerGreenstone LLC
Substance NameAMLODIPINE BESYLATE
Strength10
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/59762-2135-9





Copyright © 2007-2024 www.ndcvalidator.com