"70518-3690-0" National Drug Code (NDC)

Sucralfate 30 TABLET in 1 BLISTER PACK (70518-3690-0)
(REMEDYREPACK INC.)

NDC Code70518-3690-0
Package Description30 TABLET in 1 BLISTER PACK (70518-3690-0)
Product NDC70518-3690
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSucralfate
Non-Proprietary NameSucralfate
Dosage FormTABLET
UsageORAL
Start Marketing Date20230323
Marketing Category NameANDA
Application NumberANDA074415
ManufacturerREMEDYREPACK INC.
Substance NameSUCRALFATE
Strength1
Strength Unitg/1
Pharmacy ClassesAluminum Complex [EPC], Organometallic Compounds [CS]

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