"50090-7178-1" National Drug Code (NDC)

Famotidine 20 TABLET, FILM COATED in 1 BOTTLE (50090-7178-1)
(A-S Medication Solutions)

NDC Code50090-7178-1
Package Description20 TABLET, FILM COATED in 1 BOTTLE (50090-7178-1)
Product NDC50090-7178
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211104
Marketing Category NameANDA
Application NumberANDA215767
ManufacturerA-S Medication Solutions
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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