"37808-897-26" National Drug Code (NDC)

Rx Act Ibuprofen 1 BOTTLE in 1 CARTON (37808-897-26) > 120 mL in 1 BOTTLE
(H E B)

NDC Code37808-897-26
Package Description1 BOTTLE in 1 CARTON (37808-897-26) > 120 mL in 1 BOTTLE
Product NDC37808-897
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act Ibuprofen
Proprietary Name SuffixChildrens
Non-Proprietary NameIbuprofen
Dosage FormSUSPENSION
UsageORAL
Start Marketing Date19990106
Marketing Category NameANDA
Application NumberANDA074937
ManufacturerH E B
Substance NameIBUPROFEN
Strength100
Strength Unitmg/5mL
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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