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] |