NDC 42291-318

NDC 42291-318

NDC 42291-318 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 42291-318
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 42291-318-18 [42291031818]

Hydroxychloroquine Sulfate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040766
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-05-19
Marketing End Date2018-05-21

NDC 42291-318-50 [42291031850]

Hydroxychloroquine Sulfate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040766
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-09-10
Marketing End Date2015-02-24

NDC 42291-318-90 [42291031890]

Hydroxychloroquine Sulfate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040766
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-09-10
Marketing End Date2015-02-24

NDC 42291-318-01 [42291031801]

Hydroxychloroquine Sulfate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040766
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-05-19
Marketing End Date2018-05-21

Drug Details

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