# Cyclomydril

NDC: 0065-0359
Generic name: cyclopentolate hydrochloride and phenylephrine hydrochloride
Labeler / Manufacturer: Alcon Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 19580630

FDA application: ANDA084300

## Active ingredients

- CYCLOPENTOLATE HYDROCHLORIDE: 2 mg/mL
- PHENYLEPHRINE HYDROCHLORIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0065-0359"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0065-0359
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8268b70f-3f10-48dd-bb24-baaeb27a1325