"37808-183-83" National Drug Code (NDC)

Rx Act Ibuprofen 225 TABLET, FILM COATED in 1 BOTTLE (37808-183-83)
(H E B)

NDC Code37808-183-83
Package Description225 TABLET, FILM COATED in 1 BOTTLE (37808-183-83)
Product NDC37808-183
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act Ibuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19940204
Marketing Category NameANDA
Application NumberANDA077349
ManufacturerH E B
Substance NameIBUPROFEN
Strength200
Strength Unitmg/1

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