"70000-0201-1" National Drug Code (NDC)

Leader All Day Pain Relief 1 BOTTLE in 1 CARTON (70000-0201-1) > 200 TABLET, FILM COATED in 1 BOTTLE
(Cardinal Health 110, LLC. dba Leader)

NDC Code70000-0201-1
Package Description1 BOTTLE in 1 CARTON (70000-0201-1) > 200 TABLET, FILM COATED in 1 BOTTLE
Product NDC70000-0201
Product Type NameHUMAN OTC DRUG
Proprietary NameLeader All Day Pain Relief
Non-Proprietary NameNaproxen Sodium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20161207
Marketing Category NameANDA
Application NumberANDA074661
ManufacturerCardinal Health 110, LLC. dba Leader
Substance NameNAPROXEN SODIUM
Strength220
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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