"61919-581-60" National Drug Code (NDC)

Atenolol 60 TABLET in 1 BOTTLE (61919-581-60)
(DIRECT RX)

NDC Code61919-581-60
Package Description60 TABLET in 1 BOTTLE (61919-581-60)
Product NDC61919-581
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtenolol
Non-Proprietary NameAtenolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20170719
Marketing Category NameANDA
Application NumberANDA076900
ManufacturerDIRECT RX
Substance NameATENOLOL
Strength25
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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