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Leucovorin
Leucovorin - 25021-816-30 - (leucovorin calcium)
Drug Information of Leucovorin
| Product NDC: | 25021-816 |
| Proprietary Name: | Leucovorin |
| Non Proprietary Name: | leucovorin calcium |
| Active Ingredient(s): | 350 mg/17.5mL & nbsp; leucovorin calcium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Leucovorin
| Product NDC: | 25021-816 |
| Labeler Name: | Sagent Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200855 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120915 |
Package Information of Leucovorin
| Package NDC: | 25021-816-30 |
| Package Description: | 1 VIAL in 1 CARTON (25021-816-30) > 17.5 mL in 1 VIAL |
NDC Information of Leucovorin
| NDC Code | 25021-816-30 |
| Proprietary Name | Leucovorin |
| Package Description | 1 VIAL in 1 CARTON (25021-816-30) > 17.5 mL in 1 VIAL |
| Product NDC | 25021-816 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | leucovorin calcium |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20120915 |
| Marketing Category Name | ANDA |
| Labeler Name | Sagent Pharmaceuticals |
| Substance Name | LEUCOVORIN CALCIUM |
| Strength Number | 350 |
| Strength Unit | mg/17.5mL |
| Pharmaceutical Classes | Folate Analog [EPC],Folic Acid [Chemical/Ingredient] |
