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"70518-0461-1" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BLISTER PACK (70518-0461-1)
(REMEDYREPACK INC.)

NDC Code70518-0461-1
Package Description30 TABLET in 1 BLISTER PACK (70518-0461-1)
Product NDC70518-0461
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20170425
Marketing Category NameANDA
Application NumberANDA075805
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/70518-0461-1





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