| Product NDC: | 55390-818 |
| Proprietary Name: | Leucovorin Calcium |
| Non Proprietary Name: | Leucovorin Calcium |
| Active Ingredient(s): | 100 mg/10mL & nbsp; Leucovorin Calcium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55390-818 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089717 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960628 |
| Package NDC: | 55390-818-10 |
| Package Description: | 10 VIAL in 1 BOX (55390-818-10) > 10 mL in 1 VIAL |
| NDC Code | 55390-818-10 |
| Proprietary Name | Leucovorin Calcium |
| Package Description | 10 VIAL in 1 BOX (55390-818-10) > 10 mL in 1 VIAL |
| Product NDC | 55390-818 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Leucovorin Calcium |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19960628 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | LEUCOVORIN CALCIUM |
| Strength Number | 100 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Folate Analog [EPC],Folic Acid [Chemical/Ingredient] |