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"11673-061-82" National Drug Code (NDC)

Up And Up Famotidine 1 BOTTLE in 1 CARTON (11673-061-82) > 200 TABLET, FILM COATED in 1 BOTTLE
(Target Corporation)

NDC Code11673-061-82
Package Description1 BOTTLE in 1 CARTON (11673-061-82) > 200 TABLET, FILM COATED in 1 BOTTLE
Product NDC11673-061
Product Type NameHUMAN OTC DRUG
Proprietary NameUp And Up Famotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120503
Marketing Category NameANDA
Application NumberANDA077351
ManufacturerTarget Corporation
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/11673-061-82





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