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Galantamine Hydrobromide Oral Solution
Galantamine Hydrobromide Oral Solution - 0054-0137-49 - (Galantamine Hydrobromide Oral Solution)
Drug Information of Galantamine Hydrobromide Oral Solution
| Product NDC: | 0054-0137 |
| Proprietary Name: | Galantamine Hydrobromide Oral Solution |
| Non Proprietary Name: | Galantamine Hydrobromide Oral Solution |
| Active Ingredient(s): | 4 mg/mL & nbsp; Galantamine Hydrobromide Oral Solution |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Galantamine Hydrobromide Oral Solution
| Product NDC: | 0054-0137 |
| Labeler Name: | Roxane Laboratories, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078185 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090814 |
Package Information of Galantamine Hydrobromide Oral Solution
| Package NDC: | 0054-0137-49 |
| Package Description: | 100 mL in 1 BOTTLE (0054-0137-49) |
NDC Information of Galantamine Hydrobromide Oral Solution
| NDC Code | 0054-0137-49 |
| Proprietary Name | Galantamine Hydrobromide Oral Solution |
| Package Description | 100 mL in 1 BOTTLE (0054-0137-49) |
| Product NDC | 0054-0137 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Galantamine Hydrobromide Oral Solution |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090814 |
| Marketing Category Name | ANDA |
| Labeler Name | Roxane Laboratories, Inc |
| Substance Name | GALANTAMINE HYDROBROMIDE |
| Strength Number | 4 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
