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"70518-2469-0" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BLISTER PACK (70518-2469-0)
(REMEDYREPACK INC.)

NDC Code70518-2469-0
Package Description30 TABLET in 1 BLISTER PACK (70518-2469-0)
Product NDC70518-2469
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20191206
Marketing Category NameANDA
Application NumberANDA078916
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/70518-2469-0





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