"37808-050-60" National Drug Code (NDC)

Rx Act Ibuprofen Pm 1 BOTTLE in 1 CARTON (37808-050-60) > 20 TABLET, COATED in 1 BOTTLE
(H E B)

NDC Code37808-050-60
Package Description1 BOTTLE in 1 CARTON (37808-050-60) > 20 TABLET, COATED in 1 BOTTLE
Product NDC37808-050
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act Ibuprofen Pm
Non-Proprietary NameDiphenhydramine Citrate, Ibuprofen
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20090311
Marketing Category NameANDA
Application NumberANDA079113
ManufacturerH E B
Substance NameDIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength38; 200
Strength Unitmg/1; mg/1

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