"68788-9220-6" National Drug Code (NDC)

Famotidine 60 TABLET, FILM COATED in 1 BOTTLE (68788-9220-6)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-9220-6
Package Description60 TABLET, FILM COATED in 1 BOTTLE (68788-9220-6)
Product NDC68788-9220
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075718
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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