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"51672-2117-4" National Drug Code (NDC)

Feverall 50 BLISTER PACK in 1 CARTON (51672-2117-4) > 1 SUPPOSITORY in 1 BLISTER PACK (51672-2117-0)
(Taro Pharmaceuticals U.S.A. Inc.)

NDC Code51672-2117-4
Package Description50 BLISTER PACK in 1 CARTON (51672-2117-4) > 1 SUPPOSITORY in 1 BLISTER PACK (51672-2117-0)
Product NDC51672-2117
Product Type NameHUMAN OTC DRUG
Proprietary NameFeverall
Proprietary Name SuffixAdults
Non-Proprietary NameAcetaminophen
Dosage FormSUPPOSITORY
UsageRECTAL
Start Marketing Date20131212
Marketing Category NameNDA
Application NumberNDA018337
ManufacturerTaro Pharmaceuticals U.S.A. Inc.
Substance NameACETAMINOPHEN
Strength650
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-2117-4





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