"59368-335-01" National Drug Code (NDC)

Acid Relief 2 BOTTLE in 1 CARTON (59368-335-01) / 85 TABLET, FILM COATED in 1 BOTTLE
(Praxis, LLC)

NDC Code59368-335-01
Package Description2 BOTTLE in 1 CARTON (59368-335-01) / 85 TABLET, FILM COATED in 1 BOTTLE
Product NDC59368-335
Product Type NameHUMAN OTC DRUG
Proprietary NameAcid Relief
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230315
Marketing Category NameANDA
Application NumberANDA077351
ManufacturerPraxis, LLC
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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