ERIBULIN MESYLATE
- Product NDC
- 39822-2080
- 11-digit product format
- 398222080
- Labeler code
- 39822
- Product ID
- 39822-2080_4d3aa580-669b-dddb-e063-6294a90a1152
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eribulin mesylate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- XGen Pharmaceuticals DJB, Inc.
- Application
- ANDA219054
- Marketing category
- ANDA
- Marketing start
- 2026-04-07
- Substance
- ERIBULIN MESYLATE
- Active strength
- .5 mg/mL
- Pharmacologic classes
- Microtubule Inhibition [PE], Microtubule Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| AV9U0660CW | ERIBULIN MESYLATE | 441045-17-6 | ERIBULIN MESYLATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 39822-2080-1 | 39822208001 | 1 VIAL, SINGLE-DOSE in 1 CARTON (39822-2080-1) / 2 mL in 1 VIAL, SINGLE-DOSE | 2026-04-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ERIBULIN MESYLATE | XGen Pharmaceuticals DJB, Inc. | 2026-03-16 | HUMAN PRESCRIPTION DRUG LABEL | 1 |