"61919-257-30" National Drug Code (NDC)

Atenolol 30 TABLET in 1 BOTTLE (61919-257-30)
(Direct Rx)

NDC Code61919-257-30
Package Description30 TABLET in 1 BOTTLE (61919-257-30)
Product NDC61919-257
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtenolol
Non-Proprietary NameAtenolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA077877
ManufacturerDirect Rx
Substance NameATENOLOL
Strength50
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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