United States · FDA National Drug Code directory
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
- 60758-802_27ed7b7d-7640-4566-90f3-42a17a9d1a98
- Product NDC
- 60758-802
- Form
- SOLUTION/ DROPS
- Composition / generic term
- timolol maleate
- Labeler
- Pacific Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19970520
- Source listing expiry
- 20271231
Source-listed ingredients
- TIMOLOL MALEATE — 2.5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DROPPER in 1 CARTON (60758-802-05) / 5 mL in 1 BOTTLE, DROPPER · 60758-802-05
- 1 BOTTLE, DROPPER in 1 CARTON (60758-802-10) / 10 mL in 1 BOTTLE, DROPPER · 60758-802-10
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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