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"0135-0136-01" National Drug Code (NDC)

Panadol 1 BOTTLE in 1 CARTON (0135-0136-01) > 10 TABLET, FILM COATED in 1 BOTTLE
(GlaxoSmithKline Consumer Healthcare Holdings (US) LLC)

NDC Code0135-0136-01
Package Description1 BOTTLE in 1 CARTON (0135-0136-01) > 10 TABLET, FILM COATED in 1 BOTTLE
Product NDC0135-0136
Product Type NameHUMAN OTC DRUG
Proprietary NamePanadol
Proprietary Name SuffixExtra Strength
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110318
End Marketing Date20190531
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/0135-0136-01





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