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Levocarnitine
Levocarnitine - 50383-172-90 - (Levocarnitine)
Drug Information of Levocarnitine
| Product NDC: | 50383-172 |
| Proprietary Name: | Levocarnitine |
| Non Proprietary Name: | Levocarnitine |
| Active Ingredient(s): | 330 mg/1 & nbsp; Levocarnitine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levocarnitine
| Product NDC: | 50383-172 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018948 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20051101 |
Package Information of Levocarnitine
| Package NDC: | 50383-172-90 |
| Package Description: | 9 BLISTER PACK in 1 CARTON (50383-172-90) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Levocarnitine
| NDC Code | 50383-172-90 |
| Proprietary Name | Levocarnitine |
| Package Description | 9 BLISTER PACK in 1 CARTON (50383-172-90) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 50383-172 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levocarnitine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20051101 |
| Marketing Category Name | NDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | LEVOCARNITINE |
| Strength Number | 330 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Carnitine [Chemical/Ingredient],Carnitine Analog [EPC] |
