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Leucovorin Calcium
Leucovorin Calcium - 0703-5145-01 - (Leucovorin Calcium)
Drug Information of Leucovorin Calcium
| Product NDC: | 0703-5145 |
| Proprietary Name: | Leucovorin Calcium |
| 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, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Leucovorin Calcium
| Product NDC: | 0703-5145 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040174 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970612 |
Package Information of Leucovorin Calcium
| Package NDC: | 0703-5145-01 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (0703-5145-01) > 17.5 mL in 1 VIAL, SINGLE-USE |
NDC Information of Leucovorin Calcium
| NDC Code | 0703-5145-01 |
| Proprietary Name | Leucovorin Calcium |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0703-5145-01) > 17.5 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0703-5145 |
| 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 | 19970612 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | LEUCOVORIN CALCIUM |
| Strength Number | 350 |
| Strength Unit | mg/17.5mL |
| Pharmaceutical Classes | Folate Analog [EPC],Folic Acid [Chemical/Ingredient] |
