"51672-2114-4" National Drug Code (NDC)

Feverall 50 BLISTER PACK in 1 CARTON (51672-2114-4) > 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)
(Taro Pharmaceuticals U.S.A. Inc.)

NDC Code51672-2114-4
Package Description50 BLISTER PACK in 1 CARTON (51672-2114-4) > 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)
Product NDC51672-2114
Product Type NameHUMAN OTC DRUG
Proprietary NameFeverall
Proprietary Name SuffixInfants
Non-Proprietary NameAcetaminophen
Dosage FormSUPPOSITORY
UsageRECTAL
Start Marketing Date20131212
Marketing Category NameNDA
Application NumberNDA018337
ManufacturerTaro Pharmaceuticals U.S.A. Inc.
Substance NameACETAMINOPHEN
Strength80
Strength Unitmg/1

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