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Lithium
Lithium - 60986-1019-4 - (Lithium Bromatum)
Drug Information of Lithium
| Product NDC: | 60986-1019 |
| Proprietary Name: | Lithium |
| Non Proprietary Name: | Lithium Bromatum |
| Active Ingredient(s): | 3 [hp_X]/mL & nbsp; Lithium Bromatum |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lithium
| Product NDC: | 60986-1019 |
| Labeler Name: | Marco Pharma International LLC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19920301 |
Package Information of Lithium
| Package NDC: | 60986-1019-4 |
| Package Description: | 100 mL in 1 BOTTLE, GLASS (60986-1019-4) |
NDC Information of Lithium
| NDC Code | 60986-1019-4 |
| Proprietary Name | Lithium |
| Package Description | 100 mL in 1 BOTTLE, GLASS (60986-1019-4) |
| Product NDC | 60986-1019 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Lithium Bromatum |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19920301 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Marco Pharma International LLC. |
| Substance Name | LITHIUM BROMIDE |
| Strength Number | 3 |
| Strength Unit | [hp_X]/mL |
| Pharmaceutical Classes |
