Leucovorin Calcium
- Product NDC
- 0703-5140
- 11-digit product format
- 007035140
- Labeler code
- 0703
- Product ID
- 0703-5140_3cfde285-f9e6-4415-9e34-7016bbfc9e39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Leucovorin Calcium
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Teva Parenteral Medicines, Inc.
- Application
- ANDA081277
- Marketing category
- ANDA
- Marketing start
- 1994-02-01
- Marketing end
- 0000-00-00
- Substance
- LEUCOVORIN CALCIUM
- Active strength
- 100 mg/10mL
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0703-5140-01 | 00703514001 | 1 VIAL, SINGLE-USE in 1 CARTON (0703-5140-01) > 10 mL in 1 VIAL, SINGLE-USE | 1994-02-01 | 0000-00-00 | No | No | Current |