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"70518-3959-0" National Drug Code (NDC)

Sucralfate 30 TABLET in 1 BLISTER PACK (70518-3959-0)
(REMEDYREPACK INC.)

NDC Code70518-3959-0
Package Description30 TABLET in 1 BLISTER PACK (70518-3959-0)
Product NDC70518-3959
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSucralfate
Non-Proprietary NameSucralfate
Dosage FormTABLET
UsageORAL
Start Marketing Date20231213
Marketing Category NameANDA
Application NumberANDA215705
ManufacturerREMEDYREPACK INC.
Substance NameSUCRALFATE
Strength1
Strength Unitg/1
Pharmacy ClassesAluminum Complex [EPC], Organometallic Compounds [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3959-0





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