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"61919-782-90" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (61919-782-90)
(DIRECT RX)

NDC Code61919-782-90
Package Description90 TABLET in 1 BOTTLE (61919-782-90)
Product NDC61919-782
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20170220
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/61919-782-90





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