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"70518-1089-0" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1089-0)
(REMEDYREPACK INC.)

NDC Code70518-1089-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1089-0)
Product NDC70518-1089
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180330
Marketing Category NameANDA
Application NumberANDA075704
ManufacturerREMEDYREPACK INC.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1089-0





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