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LITHOBID
LITHOBID - 68968-4492-1 - (lithium carbonate)
Drug Information of LITHOBID
| Product NDC: | 68968-4492 |
| Proprietary Name: | LITHOBID |
| Non Proprietary Name: | lithium carbonate |
| Active Ingredient(s): | 300 mg/1 & nbsp; lithium carbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LITHOBID
| Product NDC: | 68968-4492 |
| Labeler Name: | NOVEN THERAPEUTICS, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018027 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19790427 |
Package Information of LITHOBID
| Package NDC: | 68968-4492-1 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68968-4492-1) |
NDC Information of LITHOBID
| NDC Code | 68968-4492-1 |
| Proprietary Name | LITHOBID |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68968-4492-1) |
| Product NDC | 68968-4492 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lithium carbonate |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19790427 |
| Marketing Category Name | NDA |
| Labeler Name | NOVEN THERAPEUTICS, LLC |
| Substance Name | LITHIUM CARBONATE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Mood Stabilizer [EPC] |
