Epirubicin Hydrochloride
- Product NDC
- 0115-1675
- 11-digit product format
- 001151675
- Labeler code
- 0115
- Product ID
- 0115-1675_4f954c6a-221b-494c-aea7-1a8c1b65e424
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Epirubicin Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Impax Generics
- Application
- ANDA065445
- Marketing category
- ANDA
- Marketing start
- 2016-09-21
- Marketing end
- 0000-00-00
- Substance
- EPIRUBICIN HYDROCHLORIDE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [CS],Topoisomerase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record