"61919-935-90" National Drug Code (NDC)

Atenolol 90 TABLET in 1 BOTTLE (61919-935-90)
(Direct_Rx)

NDC Code61919-935-90
Package Description90 TABLET in 1 BOTTLE (61919-935-90)
Product NDC61919-935
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtenolol
Non-Proprietary NameAtenolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20190729
Marketing Category NameANDA
Application NumberANDA076900
ManufacturerDirect_Rx
Substance NameATENOLOL
Strength50
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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