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
- 61314-396_6b554ca9-699a-4d71-8e46-0130c675ca3c
- Product NDC
- 61314-396
- Form
- SOLUTION
- Composition / generic term
- Cyclopentolate Hydrochloride
- Labeler
- Sandoz Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020822
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOPENTOLATE HYDROCHLORIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 mL in 1 BOTTLE (61314-396-01) · 61314-396-01
- 5 mL in 1 BOTTLE (61314-396-02) · 61314-396-02
- 15 mL in 1 BOTTLE (61314-396-03) · 61314-396-03
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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