PROPAFENONE HYDROCHLORIDE (Sun Pharmaceutical Industries, Inc.)
Welcome to the PulseAid listing for the PROPAFENONE HYDROCHLORIDE drug offered from Sun Pharmaceutical Industries, Inc.. This Antiarrhythmic [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Sun Pharmaceutical Industries, Inc. |
| NON-PROPRIETARY NAME: | propafenone hydrochloride |
| SUBSTANCE NAME: | PROPAFENONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Antiarrhythmic [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2001-11-29 |
| END MARKETING DATE: | 0000-00-00 |
PROPAFENONE HYDROCHLORIDE HUMAN PRESCRIPTION DRUG Details:
| Item Description | PROPAFENONE HYDROCHLORIDE from Sun Pharmaceutical Industries, Inc. |
| LABELER NAME: | Sun Pharmaceutical Industries, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 150(mg/1) |
| START MARKETING DATE: | 2001-11-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 53489-551_0a371c0c-062e-4318-bc39-447108953a8b |
| PRODUCT NDC: | 53489-551 |
| APPLICATION NUMBER: | ANDA075998 |
Other PROPAFENONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
