"72189-234-20" National Drug Code (NDC)

Sucralfate 20 TABLET in 1 BOTTLE (72189-234-20)
(DIRECT RX)

NDC Code72189-234-20
Package Description20 TABLET in 1 BOTTLE (72189-234-20)
Product NDC72189-234
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSucralfate
Non-Proprietary NameSucralfate
Dosage FormTABLET
UsageORAL
Start Marketing Date20210618
Marketing Category NameANDA
Application NumberANDA070848
ManufacturerDIRECT RX
Substance NameSUCRALFATE
Strength1
Strength Unitg/1
Pharmacy ClassesAluminum Complex [EPC], Organometallic Compounds [CS]

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