NDC 60429-502

NDC 60429-502

NDC 60429-502 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 60429-502
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 60429-502-10 [60429050210]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-03-28
Marketing End Date2017-10-10

NDC 60429-502-05 [60429050205]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-03-28
Marketing End Date2017-10-10

NDC 60429-502-90 [60429050290]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Marketing End Date2017-10-10

NDC 60429-502-12 [60429050212]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Marketing End Date2017-10-10

NDC 60429-502-15 [60429050215]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Marketing End Date2017-10-10

NDC 60429-502-01 [60429050201]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-03-28
Marketing End Date2017-10-10

NDC 60429-502-30 [60429050230]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Marketing End Date2017-10-10

NDC 60429-502-18 [60429050218]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Marketing End Date2017-10-10

NDC 60429-502-60 [60429050260]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Marketing End Date2017-10-10

Drug Details

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