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RAZADYNE
RAZADYNE - 21695-184-30 - (galantamine hydrobromide)
Drug Information of RAZADYNE
| Product NDC: | 21695-184 |
| Proprietary Name: | RAZADYNE |
| Non Proprietary Name: | galantamine hydrobromide |
| Active Ingredient(s): | 8 mg/1 & nbsp; galantamine hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RAZADYNE
| Product NDC: | 21695-184 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021169 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010228 |
Package Information of RAZADYNE
| Package NDC: | 21695-184-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (21695-184-30) |
NDC Information of RAZADYNE
| NDC Code | 21695-184-30 |
| Proprietary Name | RAZADYNE |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (21695-184-30) |
| Product NDC | 21695-184 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | galantamine hydrobromide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20010228 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | GALANTAMINE HYDROBROMIDE |
| Strength Number | 8 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
