"68788-9779-3" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (68788-9779-3)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-9779-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68788-9779-3)
Product NDC68788-9779
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120727
Marketing Category NameANDA
Application NumberANDA075786
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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