"49483-716-49" National Drug Code (NDC)

Dual Action Pain Relief 1 BOTTLE in 1 CARTON (49483-716-49) / 144 TABLET in 1 BOTTLE
(TIME CAP LABORATORIES, INC.)

NDC Code49483-716-49
Package Description1 BOTTLE in 1 CARTON (49483-716-49) / 144 TABLET in 1 BOTTLE
Product NDC49483-716
Product Type NameHUMAN OTC DRUG
Proprietary NameDual Action Pain Relief
Non-Proprietary NameAcetaminophen, Ibuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20231013
Marketing Category NameANDA
Application NumberANDA216994
ManufacturerTIME CAP LABORATORIES, 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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