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"61715-063-30" National Drug Code (NDC)

Famotidine 1 BLISTER PACK in 1 CARTON (61715-063-30) > 30 TABLET, FILM COATED in 1 BLISTER PACK
(Kinray)

NDC Code61715-063-30
Package Description1 BLISTER PACK in 1 CARTON (61715-063-30) > 30 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC61715-063
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20111003
Marketing Category NameANDA
Application NumberANDA090283
ManufacturerKinray
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61715-063-30





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