"70000-0539-1" National Drug Code (NDC)

Leader Acid Reducer 30 BLISTER PACK in 1 CARTON (70000-0539-1) > 1 TABLET, FILM COATED in 1 BLISTER PACK
(Cardinal Health 110, LLC. dba Leader)

NDC Code70000-0539-1
Package Description30 BLISTER PACK in 1 CARTON (70000-0539-1) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC70000-0539
Product Type NameHUMAN OTC DRUG
Proprietary NameLeader Acid Reducer
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200128
End Marketing Date20220531
Marketing Category NameANDA
Application NumberANDA075400
ManufacturerCardinal Health 110, LLC. dba Leader
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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