"0135-0607-02" National Drug Code (NDC)

Panadol 3 BLISTER PACK in 1 CARTON (0135-0607-02) / 8 TABLET, FILM COATED in 1 BLISTER PACK
(Haleon US Holdings LLC)

NDC Code0135-0607-02
Package Description3 BLISTER PACK in 1 CARTON (0135-0607-02) / 8 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0135-0607
Product Type NameHUMAN OTC DRUG
Proprietary NamePanadol
Proprietary Name SuffixCold And Flu Nondrowsy
Non-Proprietary NameAcetaminophen And Phenyleprine Hcl
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170601
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM013
ManufacturerHaleon US Holdings LLC
Substance NameACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength325; 5
Strength Unitmg/1; mg/1
Pharmacy ClassesAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]

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