Cyclopentolate Hydrochloride (Sandoz Inc.)
Welcome to the PulseAid listing for the Cyclopentolate Hydrochloride drug offered from Sandoz Inc.. This 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: | Sandoz Inc. |
| NON-PROPRIETARY NAME: | Cyclopentolate Hydrochloride |
| SUBSTANCE NAME: | CYCLOPENTOLATE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | OPHTHALMIC |
| DOSAGE FORM: | SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2002-08-22 |
| END MARKETING DATE: | 0000-00-00 |
Cyclopentolate Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Cyclopentolate Hydrochloride from Sandoz Inc. |
| LABELER NAME: | Sandoz Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 2002-08-22 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 61314-396_045e8129-2a07-1cfc-2d85-05ce7e8df314 |
| PRODUCT NDC: | 61314-396 |
| APPLICATION NUMBER: | ANDA084110 |
Other CYCLOPENTOLATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
