NDC 42658-021

Daunorubicin Hydrochloride

Daunorubicin Hydrochloride

Daunorubicin Hydrochloride is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hisun Pharmaceuticals Usa, Inc.. The primary component is Daunorubicin Hydrochloride.

Product ID42658-021_9ca91407-5781-1a8b-e053-2a95a90a9a31
Product TypeHuman Prescription Drug
Proprietary NameDaunorubicin Hydrochloride
Generic NameDaunorubicin Hydrochloride
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2020-01-20
Marketing CategoryANDA /
Application NumberANDA208759
Labeler NameHisun Pharmaceuticals USA, Inc.
Active Ingredient Strength5 mg/mL
Pharm ClassesAnthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [CS],Topoisomerase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31


NDC 42658-021-01

1 VIAL in 1 BOX (42658-021-01) > 4 mL in 1 VIAL
Marketing Start Date2020-01-20
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Daunorubicin Hydrochloride" or generic name "Daunorubicin Hydrochloride"

NDCBrand NameGeneric Name
0143-9550Daunorubicin HydrochlorideDaunorubicin Hydrochloride
0143-9551Daunorubicin HydrochlorideDaunorubicin Hydrochloride
0703-5233daunorubicin hydrochloridedaunorubicin hydrochloride
42658-021Daunorubicin Hydrochloridedaunorubicin hydrochloride

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.