NDC 16590-020

NDC 16590-020

NDC 16590-020 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 16590-020
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 16590-020-21 [16590002021]

AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA065093
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-11-21
Inactivation Date2019-11-13

NDC 16590-020-14 [16590002014]

AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA065093
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-11-21
Inactivation Date2019-11-13

NDC 16590-020-10 [16590002010]

AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA065093
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-11-21
Inactivation Date2019-11-13

NDC 16590-020-20 [16590002020]

AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA065093
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-11-21
Inactivation Date2019-11-13

NDC 16590-020-28 [16590002028]

AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA065093
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-11-21
Inactivation Date2019-11-13

NDC 16590-020-30 [16590002030]

AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA065093
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-11-21
Inactivation Date2019-11-13

Drug Details


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