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

Panadol 1 BOTTLE in 1 CARTON (0135-0135-02) > 30 TABLET in 1 BOTTLE
(GlaxoSmithKline Consumer Healthcare Holdings (US) LLC)

NDC Code0135-0135-02
Package Description1 BOTTLE in 1 CARTON (0135-0135-02) > 30 TABLET in 1 BOTTLE
Product NDC0135-0135
Product Type NameHUMAN OTC DRUG
Proprietary NamePanadol
Proprietary Name SuffixExtra Strength
Non-Proprietary NameAcetaminophen
Dosage FormTABLET
UsageORAL
Start Marketing Date20110318
End Marketing Date20181130
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/0135-0135-02





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