Cyclopentolate Hydrochloride (Akorn, Inc.)
Welcome to the PulseAid listing for the Cyclopentolate Hydrochloride drug offered from Akorn, 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: | Akorn, Inc. |
| NON-PROPRIETARY NAME: | Cyclopentolate Hydrochloride |
| SUBSTANCE NAME: | CYCLOPENTOLATE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | OPHTHALMIC |
| DOSAGE FORM: | SOLUTION/ DROPS |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1997-01-13 |
| END MARKETING DATE: | 0000-00-00 |
Cyclopentolate Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Cyclopentolate Hydrochloride from Akorn, Inc. |
| LABELER NAME: | Akorn, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 20(mg/mL) |
| START MARKETING DATE: | 1997-01-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 17478-097_4b3e7b47-d9d2-4c12-afb5-d42e2247608e |
| PRODUCT NDC: | 17478-097 |
| APPLICATION NUMBER: | ANDA040165 |
Other CYCLOPENTOLATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: