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"70518-1913-0" National Drug Code (NDC)

Zoloft 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1913-0)
(REMEDYREPACK INC.)

NDC Code70518-1913-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1913-0)
Product NDC70518-1913
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZoloft
Non-Proprietary NameSertraline Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190227
Marketing Category NameNDA
Application NumberNDA019839
ManufacturerREMEDYREPACK INC.
Substance NameSERTRALINE HYDROCHLORIDE
Strength50
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1913-0





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