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Calcium Folinate
Calcium Folinate - 0703-2797-01 - (Calcium Folinate)
Drug Information of Calcium Folinate
| Product NDC: | 0703-2797 |
| Proprietary Name: | Calcium Folinate |
| Non Proprietary Name: | Calcium Folinate |
| Active Ingredient(s): | 10 mg/mL & nbsp; Calcium Folinate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Calcium Folinate
| Product NDC: | 0703-2797 |
| Labeler Name: | Teva Parenteral Medicines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Start Marketing Date: | 20110712 |
Package Information of Calcium Folinate
| Package NDC: | 0703-2797-01 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-2797-01) > 30 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Calcium Folinate
| NDC Code | 0703-2797-01 |
| Proprietary Name | Calcium Folinate |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-2797-01) > 30 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0703-2797 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcium Folinate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20110712 |
| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Labeler Name | Teva Parenteral Medicines, Inc |
| Substance Name | LEUCOVORIN CALCIUM |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Folate Analog [EPC],Folic Acid [Chemical/Ingredient] |
