"61786-500-19" National Drug Code (NDC)

Atenolol 90 TABLET in 1 BOTTLE (61786-500-19)
(REMEDYREPACK INC.)

NDC Code61786-500-19
Package Description90 TABLET in 1 BOTTLE (61786-500-19)
Product NDC61786-500
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtenolol
Non-Proprietary NameAtenolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20151209
Marketing Category NameANDA
Application NumberANDA074052
ManufacturerREMEDYREPACK INC.
Substance NameATENOLOL
Strength25
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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