Sudafed12 Hour Pressure And Pain (Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division)
Welcome to the PulseAid listing for the Sudafed drug offered from Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| NON-PROPRIETARY NAME: | Naproxen sodium and Pseudoephedrine Hydrochloride |
| SUBSTANCE NAME: | NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2010-11-01 |
| END MARKETING DATE: | 0000-00-00 |
Sudafed 12 Hour Pressure And Pain HUMAN OTC DRUG Details:
| Item Description | Sudafed 12 Hour Pressure And Pain from Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| LABELER NAME: | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 220; 120(mg/1; mg/1) |
| START MARKETING DATE: | 2010-11-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50580-539_da2dd8dd-76fe-4d9c-91d7-664d5c39ff21 |
| PRODUCT NDC: | 50580-539 |
| APPLICATION NUMBER: | ANDA076518 |
Other NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
