NDC 71474-301

NDC 71474-301

NDC 71474-301 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 71474-301
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 71474-301-55 [71474030155]

keragel
Marketing CategoryEXEMPT DEVICE
Application NumberFRO
Product TypePRESCRIPTION MEDICAL DEVICE
Billing UnitGM
Marketing Start Date2017-10-03

NDC 71474-301-20 [71474030120]

keragel
Marketing CategoryEXEMPT DEVICE
Application NumberFRO
Product TypePRESCRIPTION MEDICAL DEVICE
Billing UnitGM
Marketing Start Date2009-02-11

NDC 71474-301-30 [71474030130]

keragel
Marketing CategoryEXEMPT DEVICE
Application NumberFRO
Product TypePRESCRIPTION MEDICAL DEVICE
Billing UnitGM
Marketing Start Date2009-02-11

NDC 71474-301-10 [71474030110]

keragel
Marketing CategoryEXEMPT DEVICE
Application NumberFRO
Product TypePRESCRIPTION MEDICAL DEVICE
Billing UnitGM
Marketing Start Date2009-02-11

NDC 71474-301-05 [71474030105]

keragel
Marketing CategoryEXEMPT DEVICE
Application NumberFRO
Product TypePRESCRIPTION MEDICAL DEVICE
Marketing Start Date2018-10-08

Drug Details

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.