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"0135-0507-04" National Drug Code (NDC)

Panadol 1 BOTTLE in 1 CARTON (0135-0507-04) > 20 TABLET, FILM COATED in 1 BOTTLE
(GlaxoSmithKline Consumer Healthcare Holdings (US) LLC)

NDC Code0135-0507-04
Package Description1 BOTTLE in 1 CARTON (0135-0507-04) > 20 TABLET, FILM COATED in 1 BOTTLE
Product NDC0135-0507
Product Type NameHUMAN OTC DRUG
Proprietary NamePanadol
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110621
End Marketing Date20170531
Marketing Category NameOTC MONOGRAPH NOT FINAL
Application Numberpart343
ManufacturerGlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance NameACETAMINOPHEN
Strength500
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0135-0507-04





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