NDC 16590-003

NDC 16590-003

NDC 16590-003 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 16590-003
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 16590-003-25 [16590000325]

ACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA074980
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-09-30
Inactivation Date2019-10-29

NDC 16590-003-30 [16590000330]

ACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA074980
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-09-30
Inactivation Date2019-10-29

NDC 16590-003-21 [16590000321]

ACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA074980
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-09-30
Inactivation Date2019-10-29

NDC 16590-003-35 [16590000335]

ACYCLOVIR TABLET
Marketing CategoryANDA
Application NumberANDA074980
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-09-30
Inactivation Date2019-10-29

Drug Details


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