"70518-2939-2" National Drug Code (NDC)

Atenolol 90 TABLET in 1 BOTTLE, PLASTIC (70518-2939-2)
(REMEDYREPACK INC.)

NDC Code70518-2939-2
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-2939-2)
Product NDC70518-2939
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtenolol
Non-Proprietary NameAtenolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20201111
Marketing Category NameANDA
Application NumberANDA077443
ManufacturerREMEDYREPACK INC.
Substance NameATENOLOL
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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