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"11673-031-65" National Drug Code (NDC)

Up And Up Famotidine 30 BLISTER PACK in 1 CARTON (11673-031-65) > 1 TABLET, FILM COATED in 1 BLISTER PACK
(Target Corporation)

NDC Code11673-031-65
Package Description30 BLISTER PACK in 1 CARTON (11673-031-65) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC11673-031
Product Type NameHUMAN OTC DRUG
Proprietary NameUp And Up Famotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150313
Marketing Category NameANDA
Application NumberANDA075400
ManufacturerTarget Corporation
Substance NameFAMOTIDINE
Strength10
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/11673-031-65





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