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Lithium Carbonate
Lithium Carbonate - 68084-567-01 - (Lithium Carbonate)
Drug Information of Lithium Carbonate
| Product NDC: | 68084-567 |
| 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, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lithium Carbonate
| Product NDC: | 68084-567 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091544 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120305 |
Package Information of Lithium Carbonate
| Package NDC: | 68084-567-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-567-01) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-567-11) |
NDC Information of Lithium Carbonate
| NDC Code | 68084-567-01 |
| Proprietary Name | Lithium Carbonate |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-567-01) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-567-11) |
| Product NDC | 68084-567 |
| 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 | 20120305 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | LITHIUM CARBONATE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Mood Stabilizer [EPC] |
