United States · FDA National Drug Code directory
PREDNISOLONE ACETATE
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
- 60758-119_9bb24539-c1ac-4ce6-88a8-a5dfad588c27
- Product NDC
- 60758-119
- Form
- SUSPENSION/ DROPS
- Composition / generic term
- prednisolone acetate
- Labeler
- Pacific Pharma, Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 19970819
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISOLONE ACETATE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DROPPER in 1 CARTON (60758-119-05) / 5 mL in 1 BOTTLE, DROPPER · 60758-119-05
- 1 BOTTLE, DROPPER in 1 CARTON (60758-119-10) / 10 mL in 1 BOTTLE, DROPPER · 60758-119-10
- 1 BOTTLE, DROPPER in 1 CARTON (60758-119-15) / 15 mL in 1 BOTTLE, DROPPER · 60758-119-15
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →