"64980-623-50" National Drug Code (NDC)

Famotidine 500 TABLET, FILM COATED in 1 BOTTLE (64980-623-50)
(Rising Pharma Holdings, Inc.)

NDC Code64980-623-50
Package Description500 TABLET, FILM COATED in 1 BOTTLE (64980-623-50)
Product NDC64980-623
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240506
Marketing Category NameANDA
Application NumberANDA218181
ManufacturerRising Pharma Holdings, Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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