United States · FDA National Drug Code directory
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE
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
- 42571-382_50aa565b-e11f-8176-e063-6294a90ab0b5
- Product NDC
- 42571-382
- Form
- SOLUTION/ DROPS
- Composition / generic term
- DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE PRESERVATIVE FREE
- Labeler
- Micro Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220215
- Source listing expiry
- 20271231
Source-listed ingredients
- DORZOLAMIDE HYDROCHLORIDE — 20 mg/mL
- TIMOLOL MALEATE — 5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 12 POUCH in 1 CARTON (42571-382-27) / 15 VIAL, SINGLE-USE in 1 POUCH / .2 mL in 1 VIAL, SINGLE-USE · 42571-382-27
- 4 POUCH in 1 CARTON (42571-382-73) / 15 VIAL, SINGLE-USE in 1 POUCH (42571-382-71) / .2 mL in 1 VIAL, SINGLE-USE · 42571-382-73
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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