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"37808-140-82" National Drug Code (NDC)

Rx Act All Day Pain Relief 200 TABLET, FILM COATED in 1 BOTTLE (37808-140-82)
(H E B)

NDC Code37808-140-82
Package Description200 TABLET, FILM COATED in 1 BOTTLE (37808-140-82)
Product NDC37808-140
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act All Day Pain Relief
Non-Proprietary NameNaproxen Sodium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20080212
Marketing Category NameANDA
Application NumberANDA074661
ManufacturerH E B
Substance NameNAPROXEN SODIUM
Strength220
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-140-82





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