"37808-490-71" National Drug Code (NDC)

Rx Act All Day Pain Relief 1 BOTTLE in 1 CARTON (37808-490-71) > 50 TABLET in 1 BOTTLE
(H E B)

NDC Code37808-490-71
Package Description1 BOTTLE in 1 CARTON (37808-490-71) > 50 TABLET in 1 BOTTLE
Product NDC37808-490
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act All Day Pain Relief
Non-Proprietary NameNaproxen Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date19970224
Marketing Category NameANDA
Application NumberANDA074661
ManufacturerH E B
Substance NameNAPROXEN SODIUM
Strength220
Strength Unitmg/1

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