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galantamine hydrobromide
galantamine hydrobromide - 10147-0892-3 - (galantamine hydrobromide)
Drug Information of galantamine hydrobromide
| Product NDC: | 10147-0892 |
| Proprietary Name: | galantamine hydrobromide |
| Non Proprietary Name: | galantamine hydrobromide |
| Active Ingredient(s): | 16 mg/1 & nbsp; galantamine hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of galantamine hydrobromide
| Product NDC: | 10147-0892 |
| Labeler Name: | Patriot Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021615 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20041222 |
Package Information of galantamine hydrobromide
| Package NDC: | 10147-0892-3 |
| Package Description: | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10147-0892-3) |
NDC Information of galantamine hydrobromide
| NDC Code | 10147-0892-3 |
| Proprietary Name | galantamine hydrobromide |
| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10147-0892-3) |
| Product NDC | 10147-0892 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | galantamine hydrobromide |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20041222 |
| Marketing Category Name | NDA |
| Labeler Name | Patriot Pharmaceuticals, LLC |
| Substance Name | GALANTAMINE HYDROBROMIDE |
| Strength Number | 16 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
