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"49349-017-02" National Drug Code (NDC)

Sucralfate 30 TABLET in 1 BLISTER PACK (49349-017-02)
(REMEDYREPACK INC.)

NDC Code49349-017-02
Package Description30 TABLET in 1 BLISTER PACK (49349-017-02)
Product NDC49349-017
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSucralfate
Non-Proprietary NameSucralfate
Dosage FormTABLET
UsageORAL
Start Marketing Date20100929
Marketing Category NameNDA
Application NumberNDA018333
ManufacturerREMEDYREPACK INC.
Substance NameSUCRALFATE
Strength1
Strength Unitg/1
Pharmacy ClassesAluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-017-02





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