"79481-0152-0" National Drug Code (NDC)

Dual Action Back Pain Reliever 1 BOTTLE in 1 CARTON (79481-0152-0) / 72 TABLET, FILM COATED in 1 BOTTLE (79481-0152-1)
(Meijer, Inc.)

NDC Code79481-0152-0
Package Description1 BOTTLE in 1 CARTON (79481-0152-0) / 72 TABLET, FILM COATED in 1 BOTTLE (79481-0152-1)
Product NDC79481-0152
Product Type NameHUMAN OTC DRUG
Proprietary NameDual Action Back Pain Reliever
Non-Proprietary NameAcetaminophen, Ibuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260305
Marketing Category NameANDA
Application NumberANDA214836
ManufacturerMeijer, Inc.
Substance NameACETAMINOPHEN; IBUPROFEN
Strength250; 125
Strength Unitmg/1; mg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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