"61919-782-30" National Drug Code (NDC)

Amlodipine Besylate 30 TABLET in 1 BOTTLE (61919-782-30)
(Direct_Rx)

NDC Code61919-782-30
Package Description30 TABLET in 1 BOTTLE (61919-782-30)
Product NDC61919-782
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20190729
Marketing Category NameANDA
Application NumberANDA203245
ManufacturerDirect_Rx
Substance NameAMLODIPINE BESYLATE
Strength10
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-782-30