Fusilev
- Product NDC
- 72893-009
- 11-digit product format
- 728930009
- Labeler code
- 72893
- Product ID
- 72893-009_7c7edc08-5f57-4ef5-961c-07c17480fad3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levoleucovorin
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Acrotech Biopharma LLC
- Application
- NDA020140
- Marketing category
- NDA
- Marketing start
- 2008-08-15
- Marketing end
- 0000-00-00
- Substance
- LEVOLEUCOVORIN CALCIUM
- Active strength
- 50 mg/5mL
- Pharmacologic classes
- Folate Analog [EPC],Folic Acid [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72893-009-01 | 72893000901 | 1 VIAL in 1 CARTON (72893-009-01) > 5 mL in 1 VIAL | 1 vial | 2008-08-15 | 0000-00-00 | No | No | Current |