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Lithium Citrate
Lithium Citrate - 68094-767-62 - (Lithium Citrate)
Drug Information of Lithium Citrate
| Product NDC: | 68094-767 |
| Proprietary Name: | Lithium Citrate |
| Non Proprietary Name: | Lithium Citrate |
| Active Ingredient(s): | 8 meq/5mL & nbsp; Lithium Citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lithium Citrate
| Product NDC: | 68094-767 |
| Labeler Name: | Precision Dose Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070755 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090929 |
Package Information of Lithium Citrate
| Package NDC: | 68094-767-62 |
| Package Description: | 3 TRAY in 1 CASE (68094-767-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-767-59) |
NDC Information of Lithium Citrate
| NDC Code | 68094-767-62 |
| Proprietary Name | Lithium Citrate |
| Package Description | 3 TRAY in 1 CASE (68094-767-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-767-59) |
| Product NDC | 68094-767 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lithium Citrate |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20090929 |
| Marketing Category Name | ANDA |
| Labeler Name | Precision Dose Inc. |
| Substance Name | LITHIUM CITRATE |
| Strength Number | 8 |
| Strength Unit | meq/5mL |
| Pharmaceutical Classes | Mood Stabilizer [EPC] |
