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"71335-2190-1" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (71335-2190-1)
(Bryant Ranch Prepack)

NDC Code71335-2190-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (71335-2190-1)
Product NDC71335-2190
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220606
Marketing Category NameANDA
Application NumberANDA216441
ManufacturerBryant Ranch Prepack
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2190-1





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