rx act ibuprofen pm (H E B)
Welcome to the PulseAid listing for the rx act ibuprofen pm drug offered from H E B. 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: | H E B |
| NON-PROPRIETARY NAME: | diphenhydramine citrate, ibuprofen |
| SUBSTANCE NAME: | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2009-03-11 |
| END MARKETING DATE: | 0000-00-00 |
rx act ibuprofen pm HUMAN OTC DRUG Details:
| Item Description | rx act ibuprofen pm from H E B |
| LABELER NAME: | H E B |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 38; 200(mg/1; mg/1) |
| START MARKETING DATE: | 2009-03-11 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 37808-050_f341b4ca-dae3-4a0d-b64d-10f29528be48 |
| PRODUCT NDC: | 37808-050 |
| APPLICATION NUMBER: | ANDA079113 |
Other DIPHENHYDRAMINE CITRATE; IBUPROFEN Pharmaceutical Manufacturers / Labelers:
