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"11673-201-65" National Drug Code (NDC)

Up And Up Acid Reducer 3 BLISTER PACK in 1 CARTON (11673-201-65) > 10 TABLET in 1 BLISTER PACK
(Target Corporation)

NDC Code11673-201-65
Package Description3 BLISTER PACK in 1 CARTON (11673-201-65) > 10 TABLET in 1 BLISTER PACK
Product NDC11673-201
Product Type NameHUMAN OTC DRUG
Proprietary NameUp And Up Acid Reducer
Proprietary Name SuffixOriginal Strength
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20091013
Marketing Category NameANDA
Application NumberANDA075400
ManufacturerTarget Corporation
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/11673-201-65





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