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: