Product NDC: | 55154-4952 |
Proprietary Name: | Lithium |
Non Proprietary Name: | Lithium Carbonate |
Active Ingredient(s): | 8 meq/5mL & nbsp; Lithium Carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-4952 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018421 |
Marketing Category: | NDA |
Start Marketing Date: | 19820429 |
Package NDC: | 55154-4952-5 |
Package Description: | 5 CUP, UNIT-DOSE in 1 BAG (55154-4952-5) > 5 mL in 1 CUP, UNIT-DOSE |
NDC Code | 55154-4952-5 |
Proprietary Name | Lithium |
Package Description | 5 CUP, UNIT-DOSE in 1 BAG (55154-4952-5) > 5 mL in 1 CUP, UNIT-DOSE |
Product NDC | 55154-4952 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lithium Carbonate |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19820429 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | LITHIUM CARBONATE |
Strength Number | 8 |
Strength Unit | meq/5mL |
Pharmaceutical Classes | Mood Stabilizer [EPC] |