"70786-0121-1" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BOTTLE (70786-0121-1)
(Unit Dose Services)

NDC Code70786-0121-1
Package Description30 TABLET in 1 BOTTLE (70786-0121-1)
Product NDC70786-0121
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerUnit Dose Services
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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