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"70934-877-90" National Drug Code (NDC)

Famotidine 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-877-90)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-877-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-877-90)
Product NDC70934-877
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210730
End Marketing Date20230930
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameFAMOTIDINE
Strength40
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/70934-877-90





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