NDC 50090-1867

NDC 50090-1867

NDC 50090-1867 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 50090-1867
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 50090-1867-0 [50090186700]

Allopurinol TABLET
Marketing CategoryNDA
Application NumberNDA018877
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-06-09
Marketing End Date2019-11-30

NDC 50090-1867-3 [50090186703]

Allopurinol TABLET
Marketing CategoryNDA
Application NumberNDA018877
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-06-09
Marketing End Date2019-11-30

NDC 50090-1867-1 [50090186701]

Allopurinol TABLET
Marketing CategoryNDA
Application NumberNDA018877
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-06-09
Marketing End Date2019-11-30

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.