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"67877-626-06" National Drug Code (NDC)

Ibuprofen And Famotidine 6 BLISTER PACK in 1 CARTON (67877-626-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK
(Ascend Laboratories, LLC)

NDC Code67877-626-06
Package Description6 BLISTER PACK in 1 CARTON (67877-626-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC67877-626
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen And Famotidine
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210804
Marketing Category NameANDA
Application NumberANDA211890
ManufacturerAscend Laboratories, LLC
Substance NameFAMOTIDINE; IBUPROFEN
Strength26.6; 800
Strength Unitmg/1; mg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67877-626-06





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