NDC 0406-1772

NDC 0406-1772

NDC 0406-1772 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0406-1772
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0406-1772-33 [00406177233]

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA075738
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-08
Marketing End Date2009-08-20

NDC 0406-1772-10 [00406177210]

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA075738
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-08
Marketing End Date2011-07-31

NDC 0406-1772-01 [00406177201]

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA075738
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-08
Marketing End Date2011-07-31

NDC 0406-1772-05 [00406177205]

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA075738
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-08
Marketing End Date2011-07-31

NDC 0406-1772-62 [00406177262]

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA075738
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-08
Marketing End Date2011-07-31

NDC 0406-1772-12 [00406177212]

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA075738
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-08
Marketing End Date2009-08-20

Drug Details


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