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LITHIUM CARBONATE
LITHIUM CARBONATE - 16590-781-30 - (LITHIUM CARBONATE)
Drug Information of LITHIUM CARBONATE
| Product NDC: | 16590-781 |
| 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): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LITHIUM CARBONATE
| Product NDC: | 16590-781 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018558 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19820129 |
Package Information of LITHIUM CARBONATE
| Package NDC: | 16590-781-30 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (16590-781-30) |
NDC Information of LITHIUM CARBONATE
| NDC Code | 16590-781-30 |
| Proprietary Name | LITHIUM CARBONATE |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (16590-781-30) |
| Product NDC | 16590-781 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LITHIUM CARBONATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19820129 |
| Marketing Category Name | NDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | LITHIUM CARBONATE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Mood Stabilizer [EPC] |
