NDC 0135-0135

NDC 0135-0135

NDC 0135-0135 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0135-0135
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0135-0135-04 [00135013504]

PANADOL Extra Strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-18
Marketing End Date2016-12-31

NDC 0135-0135-01 [00135013501]

PANADOL Extra Strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-18
Marketing End Date2014-02-16

NDC 0135-0135-05 [00135013505]

PANADOL Extra Strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-18
Marketing End Date2018-11-30

NDC 0135-0135-02 [00135013502]

PANADOL Extra Strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-18
Marketing End Date2017-04-30

NDC 0135-0135-03 [00135013503]

PANADOL Extra Strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-18
Marketing End Date2016-12-31

NDC 0135-0135-07 [00135013507]

PANADOL Extra Strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-09-10
Marketing End Date2018-11-30

Drug Details

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