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Flecainide Acetate
Flecainide Acetate - 54868-5074-3 - (Flecainide Acetate)
Drug Information of Flecainide Acetate
| Product NDC: | 54868-5074 |
| Proprietary Name: | Flecainide Acetate |
| Non Proprietary Name: | Flecainide Acetate |
| Active Ingredient(s): | 50 mg/1 & nbsp; Flecainide Acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flecainide Acetate
| Product NDC: | 54868-5074 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076278 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040630 |
Package Information of Flecainide Acetate
| Package NDC: | 54868-5074-3 |
| Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (54868-5074-3) |
NDC Information of Flecainide Acetate
| NDC Code | 54868-5074-3 |
| Proprietary Name | Flecainide Acetate |
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (54868-5074-3) |
| Product NDC | 54868-5074 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flecainide Acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040630 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | FLECAINIDE ACETATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
