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"0135-0459-02" National Drug Code (NDC)

Panadol 3 BLISTER PACK in 1 CARTON (0135-0459-02) > 8 TABLET, FILM COATED in 1 BLISTER PACK
(GlaxoSmithKline Consumer Healthcare Holdings (US) LLC)

NDC Code0135-0459-02
Package Description3 BLISTER PACK in 1 CARTON (0135-0459-02) > 8 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0135-0459
Product Type NameHUMAN OTC DRUG
Proprietary NamePanadol
Proprietary Name SuffixCold And Flu Nondrowsy
Non-Proprietary NameAcetaminophen And Phenylephrine Hcl
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110831
End Marketing Date20170630
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart341
ManufacturerGlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance NameACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength500; 5
Strength Unitmg/1; mg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0135-0459-02





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