NDC Code | 70436-119-80 |
Package Description | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-119-80) |
Product NDC | 70436-119 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Leucovorin Calcium |
Non-Proprietary Name | Leucovorin Calcium |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20241227 |
Marketing Category Name | ANDA |
Application Number | ANDA217021 |
Manufacturer | Slate Run Pharmaceuticals, LLC |
Substance Name | LEUCOVORIN CALCIUM |
Strength | 350 |
Strength Unit | mg/1 |
Pharmacy Classes | Folate Analog [EPC], Folic Acid [CS] |