"70000-0710-1" National Drug Code (NDC)

Famotidine 1 BOTTLE in 1 CARTON (70000-0710-1) / 200 TABLET, FILM COATED in 1 BOTTLE
(LEADER/ Cardinal Health 110, Inc.)

NDC Code70000-0710-1
Package Description1 BOTTLE in 1 CARTON (70000-0710-1) / 200 TABLET, FILM COATED in 1 BOTTLE
Product NDC70000-0710
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20241204
Marketing Category NameANDA
Application NumberANDA218003
ManufacturerLEADER/ Cardinal Health 110, Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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