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"21130-039-09" National Drug Code (NDC)

Famotidine 1 BOTTLE in 1 CARTON (21130-039-09) / 30 TABLET, FILM COATED in 1 BOTTLE
(Better Living Brands LLC)

NDC Code21130-039-09
Package Description1 BOTTLE in 1 CARTON (21130-039-09) / 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC21130-039
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230908
Marketing Category NameANDA
Application NumberANDA206531
ManufacturerBetter Living Brands LLC
Substance NameFAMOTIDINE
Strength10
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/21130-039-09





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