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Leucovorin Calcium
Leucovorin Calcium - 63323-710-50 - (LEUCOVORIN CALCIUM)
Drug Information of Leucovorin Calcium
| Product NDC: | 63323-710 |
| Proprietary Name: | Leucovorin Calcium |
| Non Proprietary Name: | LEUCOVORIN CALCIUM |
| Active Ingredient(s): | 200 mg/20mL & nbsp; LEUCOVORIN CALCIUM |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Leucovorin Calcium
| Product NDC: | 63323-710 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040258 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100918 |
Package Information of Leucovorin Calcium
| Package NDC: | 63323-710-50 |
| Package Description: | 1 VIAL in 1 BOX (63323-710-50) > 20 mL in 1 VIAL |
NDC Information of Leucovorin Calcium
| NDC Code | 63323-710-50 |
| Proprietary Name | Leucovorin Calcium |
| Package Description | 1 VIAL in 1 BOX (63323-710-50) > 20 mL in 1 VIAL |
| Product NDC | 63323-710 |
| 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 | 20100918 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | LEUCOVORIN CALCIUM |
| Strength Number | 200 |
| Strength Unit | mg/20mL |
| Pharmaceutical Classes |
