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Levocarnitine
Levocarnitine - 0517-1045-25 - (Levocarnitine)
Drug Information of Levocarnitine
| Product NDC: | 0517-1045 |
| Proprietary Name: | Levocarnitine |
| Non Proprietary Name: | Levocarnitine |
| Active Ingredient(s): | 200 mg/mL & nbsp; Levocarnitine |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levocarnitine
| Product NDC: | 0517-1045 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075861 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20011008 |
Package Information of Levocarnitine
| Package NDC: | 0517-1045-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-1045-25) > 5 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Levocarnitine
| NDC Code | 0517-1045-25 |
| Proprietary Name | Levocarnitine |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-1045-25) > 5 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-1045 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levocarnitine |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20011008 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | LEVOCARNITINE |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Carnitine [Chemical/Ingredient],Carnitine Analog [EPC] |
