GenTealSevere (Novartis Pharmaceuticals Corporation)
Welcome to the PulseAid listing for the GenTeal drug offered from Novartis Pharmaceuticals Corporation. 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: | Novartis Pharmaceuticals Corporation |
| NON-PROPRIETARY NAME: | HYPROMELLOSE |
| SUBSTANCE NAME: | HYPROMELLOSE 2910 (4000 MPA.S) |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | OPHTHALMIC |
| DOSAGE FORM: | GEL |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2009-09-14 |
| END MARKETING DATE: | 0000-00-00 |
GenTeal Severe HUMAN OTC DRUG Details:
| Item Description | GenTeal Severe from Novartis Pharmaceuticals Corporation |
| LABELER NAME: | Novartis Pharmaceuticals Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.003(g/g) |
| START MARKETING DATE: | 2009-09-14 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0078-0429_6e8fbf40-9e2b-f93c-71b9-9f7b1fc36429 |
| PRODUCT NDC: | 0078-0429 |
| APPLICATION NUMBER: | part349 |
Other HYPROMELLOSE 2910 (4000 MPA.S) Pharmaceutical Manufacturers / Labelers:
