| Product NDC: | 55390-136 |
| Proprietary Name: | Levocarnitine |
| Non Proprietary Name: | Levocarnitine |
| Active Ingredient(s): | 1 g/5mL & nbsp; Levocarnitine |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55390-136 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075567 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010423 |
| Package NDC: | 55390-136-05 |
| Package Description: | 10 VIAL in 1 BOX (55390-136-05) > 5 mL in 1 VIAL |
| NDC Code | 55390-136-05 |
| Proprietary Name | Levocarnitine |
| Package Description | 10 VIAL in 1 BOX (55390-136-05) > 5 mL in 1 VIAL |
| Product NDC | 55390-136 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levocarnitine |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20010423 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | LEVOCARNITINE |
| Strength Number | 1 |
| Strength Unit | g/5mL |
| Pharmaceutical Classes | Carnitine [Chemical/Ingredient],Carnitine Analog [EPC] |