"53808-0797-1" National Drug Code (NDC)

Sucralfate 30 TABLET in 1 BLISTER PACK (53808-0797-1)
(State of Florida DOH Central Pharmacy)

NDC Code53808-0797-1
Package Description30 TABLET in 1 BLISTER PACK (53808-0797-1)
Product NDC53808-0797
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSucralfate
Non-Proprietary NameSucralfate
Dosage FormTABLET
UsageORAL
Start Marketing Date20090701
Marketing Category NameANDA
Application NumberANDA070848
ManufacturerState of Florida DOH Central Pharmacy
Substance NameSUCRALFATE
Strength1
Strength Unitg/1
Pharmacy ClassesAluminum Complex [EPC],Organometallic Compounds [CS]

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