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"61919-935-30" National Drug Code (NDC)

Atenolol 30 TABLET in 1 BOTTLE (61919-935-30)
(DIRECT RX)

NDC Code61919-935-30
Package Description30 TABLET in 1 BOTTLE (61919-935-30)
Product NDC61919-935
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtenolol
Non-Proprietary NameAtenolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20170224
Marketing Category NameANDA
Application NumberANDA076900
ManufacturerDIRECT RX
Substance NameATENOLOL
Strength50
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-935-30





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