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RYTHMOL
RYTHMOL - 0173-0794-20 - (propafenone hydrochloride)
Drug Information of RYTHMOL
| Product NDC: | 0173-0794 |
| Proprietary Name: | RYTHMOL |
| Non Proprietary Name: | propafenone hydrochloride |
| Active Ingredient(s): | 225 mg/1 & nbsp; propafenone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RYTHMOL
| Product NDC: | 0173-0794 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019151 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100104 |
Package Information of RYTHMOL
| Package NDC: | 0173-0794-20 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0173-0794-20) |
NDC Information of RYTHMOL
| NDC Code | 0173-0794-20 |
| Proprietary Name | RYTHMOL |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0173-0794-20) |
| Product NDC | 0173-0794 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | propafenone hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100104 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | PROPAFENONE HYDROCHLORIDE |
| Strength Number | 225 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
