LEUCOVORIN CALCIUM
- Product NDC
- 50742-464
- 11-digit product format
- 507420464
- Labeler code
- 50742
- Product ID
- 50742-464_e15b505a-a8ba-465d-82c2-3de48e83f834
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEUCOVORIN CALCIUM
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA210917
- Marketing category
- ANDA
- Marketing start
- 2018-11-23
- Marketing end
- 0000-00-00
- Substance
- LEUCOVORIN CALCIUM
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Folate Analog [EPC],Folic Acid [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-464-50 | 50742046450 | 1 VIAL, SINGLE-DOSE in 1 CARTON (50742-464-50) > 50 mL in 1 VIAL, SINGLE-DOSE | 2018-11-23 | 0000-00-00 | No | No | Current |