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"37808-368-79" National Drug Code (NDC)

Rx Act All Day Pain Relief 400 TABLET, FILM COATED in 1 BOTTLE (37808-368-79)
(H E B)

NDC Code37808-368-79
Package Description400 TABLET, FILM COATED in 1 BOTTLE (37808-368-79)
Product NDC37808-368
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act All Day Pain Relief
Non-Proprietary NameNaproxen Sodium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20090212
Marketing Category NameANDA
Application NumberANDA074661
ManufacturerH E B
Substance NameNAPROXEN SODIUM
Strength220
Strength Unitmg/1

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