Product NDC: | 64980-503 |
Proprietary Name: | Levocarnitine |
Non Proprietary Name: | Levocarnitine |
Active Ingredient(s): | 1 g/10mL & nbsp; Levocarnitine |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64980-503 |
Labeler Name: | Rising Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076851 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040920 |
Package NDC: | 64980-503-12 |
Package Description: | 118 mL in 1 BOTTLE, PLASTIC (64980-503-12) |
NDC Code | 64980-503-12 |
Proprietary Name | Levocarnitine |
Package Description | 118 mL in 1 BOTTLE, PLASTIC (64980-503-12) |
Product NDC | 64980-503 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Levocarnitine |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20040920 |
Marketing Category Name | ANDA |
Labeler Name | Rising Pharmaceuticals, Inc. |
Substance Name | LEVOCARNITINE |
Strength Number | 1 |
Strength Unit | g/10mL |
Pharmaceutical Classes | Carnitine [Chemical/Ingredient],Carnitine Analog [EPC] |