Leucovorin
- Product NDC
- 68001-286
- 11-digit product format
- 680010286
- Labeler code
- 68001
- Product ID
- 68001-286_f73c5c51-46ca-4669-8b7e-f76d964e6696
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Leucovorin Calcium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- BluePoint Laboratories
- Application
- ANDA200855
- Marketing category
- ANDA
- Marketing start
- 2016-07-01
- Marketing end
- 0000-00-00
- Substance
- LEUCOVORIN CALCIUM
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Folate Analog [EPC],Folic Acid [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-286-38 | 68001028638 | 1 VIAL in 1 CARTON (68001-286-38) > 17.5 mL in 1 VIAL (68001-286-39) | 1 vial | 2016-07-01 | 0000-00-00 | No | No | Current |