United States · FDA National Drug Code directory
Cyclomydril
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0065-0359_3c5dad7d-4db2-4615-92cb-01ea4d769adf
- Product NDC
- 0065-0359
- Form
- SOLUTION/ DROPS
- Composition / generic term
- cyclopentolate hydrochloride and phenylephrine hydrochloride
- Labeler
- Alcon Laboratories, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19580630
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOPENTOLATE HYDROCHLORIDE — 2 mg/mL
- PHENYLEPHRINE HYDROCHLORIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 mL in 1 BOTTLE, PLASTIC (0065-0359-02) · 0065-0359-02
- 5 mL in 1 BOTTLE, PLASTIC (0065-0359-05) · 0065-0359-05
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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