"16837-872-31" National Drug Code (NDC)

Pepcid Ac 4 BLISTER PACK in 1 CARTON (16837-872-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Johnson & Johnson Consumer Inc.)

NDC Code16837-872-31
Package Description4 BLISTER PACK in 1 CARTON (16837-872-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC16837-872
Product Type NameHUMAN OTC DRUG
Proprietary NamePepcid Ac
Proprietary Name SuffixOriginal Strength
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19951001
Marketing Category NameNDA
Application NumberNDA020325
ManufacturerJohnson & Johnson Consumer Inc.
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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