"68016-096-30" National Drug Code (NDC)

Famotidine 1 BOTTLE in 1 CARTON (68016-096-30) > 30 TABLET, FILM COATED in 1 BOTTLE
(Chain Drug Consortium, LLC)

NDC Code68016-096-30
Package Description1 BOTTLE in 1 CARTON (68016-096-30) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC68016-096
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190816
End Marketing Date20240430
Marketing Category NameANDA
Application NumberANDA206531
ManufacturerChain Drug Consortium, LLC
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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