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"70518-0770-0" National Drug Code (NDC)

Thioridazine Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0770-0)
(REMEDYREPACK INC.)

NDC Code70518-0770-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0770-0)
Product NDC70518-0770
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameThioridazine Hydrochloride
Non-Proprietary NameThioridazine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171009
Marketing Category NameANDA
Application NumberANDA088004
ManufacturerREMEDYREPACK INC.
Substance NameTHIORIDAZINE HYDROCHLORIDE
Strength50
Strength Unitmg/1
Pharmacy ClassesPhenothiazine [EPC],Phenothiazines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0770-0





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