CYCLOMYDRIL (CYCLOPENTOLATE HYDROCHLORIDE AND PHENYLEPHRINE HYDROCHLORIDE)
Summary
FDA approved CYCLOMYDRIL (CYCLOPENTOLATE HYDROCHLORIDE AND PHENYLEPHRINE HYDROCHLORIDE) by ALCON LABS INC. ANDA (Generic) approval (Labeling) on 2025-05-02. SOLUTION/DROPS, OPHTHALMIC.
Details
Source
Drug Approval
External ID
ANDA084300-44
Action Date
2025-05-02
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
CYCLOMYDRIL (generic: CYCLOPENTOLATE HYDROCHLORIDE AND PHENYLEPHRINE HYDROCHLORIDE), SOLUTION/DROPS, OPHTHALMIC. Application: ANDA084300
Company
Context & Analysis
ALCON LABS INC has 7 FDA actions in our database.
Frequently Asked Questions
How often does ALCON LABS INC have FDA actions?
ALCON LABS INC has 7 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA084300-44" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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