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"67877-843-05" National Drug Code (NDC)

Famotidine 500 TABLET, FILM COATED in 1 BOTTLE (67877-843-05)
(Ascend Laboratories, LLC)

NDC Code67877-843-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (67877-843-05)
Product NDC67877-843
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220708
Marketing Category NameANDA
Application NumberANDA215630
ManufacturerAscend Laboratories, LLC
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/67877-843-05





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