Product NDC: | 67046-430 |
Proprietary Name: | Lithium Carbonate |
Non Proprietary Name: | Lithium Carbonate |
Active Ingredient(s): | 300 mg/1 & nbsp; Lithium Carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, GELATIN COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67046-430 |
Labeler Name: | Contract Pharmacy Services-PA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017812 |
Marketing Category: | NDA |
Start Marketing Date: | 20100406 |
Package NDC: | 67046-430-30 |
Package Description: | 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (67046-430-30) |
NDC Code | 67046-430-30 |
Proprietary Name | Lithium Carbonate |
Package Description | 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (67046-430-30) |
Product NDC | 67046-430 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lithium Carbonate |
Dosage Form Name | CAPSULE, GELATIN COATED |
Route Name | ORAL |
Start Marketing Date | 20100406 |
Marketing Category Name | NDA |
Labeler Name | Contract Pharmacy Services-PA |
Substance Name | LITHIUM CARBONATE |
Strength Number | 300 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Mood Stabilizer [EPC] |