NDC 42291-617

NDC 42291-617

NDC 42291-617 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 42291-617
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 42291-617-90 [42291061790]

MIDODRINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA076449
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-03-03
Marketing End Date2015-01-06

Drug Details


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