United States · FDA National Drug Code directory
Cyclopentolate Hydrochloride
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
- 24208-735_34fff06e-fa45-478a-b136-e019483fa07d
- Product NDC
- 24208-735
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Cyclopentolate Hydrochloride
- Labeler
- Bausch & Lomb Incorporated
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19940429
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOPENTOLATE HYDROCHLORIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DROPPER in 1 CARTON (24208-735-01) / 2 mL in 1 BOTTLE, DROPPER · 24208-735-01
- 1 BOTTLE, DROPPER in 1 CARTON (24208-735-06) / 15 mL in 1 BOTTLE, DROPPER · 24208-735-06
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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