"68001-240-00" National Drug Code (NDC)

Famotidine 100 TABLET in 1 BOTTLE (68001-240-00)
(BluePoint Laboratories)

NDC Code68001-240-00
Package Description100 TABLET in 1 BOTTLE (68001-240-00)
Product NDC68001-240
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160129
End Marketing Date20220531
Marketing Category NameANDA
Application NumberANDA078916
ManufacturerBluePoint Laboratories
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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