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"58602-705-12" National Drug Code (NDC)

Famotidine 4 BLISTER PACK in 1 CARTON (58602-705-12) > 10 TABLET, FILM COATED in 1 BLISTER PACK (58602-705-03)
(Aurohealth LLC)

NDC Code58602-705-12
Package Description4 BLISTER PACK in 1 CARTON (58602-705-12) > 10 TABLET, FILM COATED in 1 BLISTER PACK (58602-705-03)
Product NDC58602-705
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160426
Marketing Category NameANDA
Application NumberANDA206531
ManufacturerAurohealth LLC
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/58602-705-12





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