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"69517-109-04" National Drug Code (NDC)

All Day Pain Relief 400 BOTTLE in 1 BOTTLE (69517-109-04) > 100 BOTTLE in 1 BOTTLE (69517-109-01) > 24 CARTON in 1 BOTTLE (69517-109-24) > 1 TABLET in 1 CARTON
(HealthLife of USA LLC)

NDC Code69517-109-04
Package Description400 BOTTLE in 1 BOTTLE (69517-109-04) > 100 BOTTLE in 1 BOTTLE (69517-109-01) > 24 CARTON in 1 BOTTLE (69517-109-24) > 1 TABLET in 1 CARTON
Product NDC69517-109
Product Type NameHUMAN OTC DRUG
Proprietary NameAll Day Pain Relief
Non-Proprietary NameNaproxen Sodium Tablets, 220 Mg
Dosage FormTABLET
UsageORAL
Start Marketing Date20110930
Marketing Category NameANDA
Application NumberANDA091353
ManufacturerHealthLife of USA LLC
Substance NameNAPROXEN SODIUM
Strength220
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69517-109-04





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