NDC 58118-0019

NDC 58118-0019

NDC 58118-0019 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 58118-0019
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 58118-0019-7 [58118001907]

Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION
Marketing CategoryANDA
Application NumberANDA050755
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-11-25
Marketing End Date2016-08-08

NDC 58118-0019-2 [58118001902]

Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION
Marketing CategoryANDA
Application NumberANDA050755
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-11-25
Marketing End Date2016-08-08

NDC 58118-0019-5 [58118001905]

Amoxicillin and Clavulanate Potassium POWDER, FOR SUSPENSION
Marketing CategoryANDA
Application NumberANDA050755
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-11-25
Marketing End Date2016-08-08

Drug Details

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