Product NDC: | 55390-051 |
Proprietary Name: | Leucovorin Calcium |
Non Proprietary Name: | Leucovorin Calcium |
Active Ingredient(s): | 50 mg/5mL & nbsp; Leucovorin Calcium |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55390-051 |
Labeler Name: | Bedford Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089384 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960501 |
Package NDC: | 55390-051-10 |
Package Description: | 10 VIAL in 1 BOX (55390-051-10) > 5 mL in 1 VIAL |
NDC Code | 55390-051-10 |
Proprietary Name | Leucovorin Calcium |
Package Description | 10 VIAL in 1 BOX (55390-051-10) > 5 mL in 1 VIAL |
Product NDC | 55390-051 |
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 | 19960501 |
Marketing Category Name | ANDA |
Labeler Name | Bedford Laboratories |
Substance Name | LEUCOVORIN CALCIUM |
Strength Number | 50 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Folate Analog [EPC],Folic Acid [Chemical/Ingredient] |