NDC 61314-637 – Prednisolone Acetate

Prednisolone Acetate 10 mg/mL · Suspension/ Drops · Ophthalmic

Human Prescription Drug 1 recall

Product NDC61314-637

Product details

Brand name
Prednisolone Acetate
Generic name
Prednisolone Acetate
Labeler
Sandoz Inc
Dosage form
Suspension/ Drops
Route
Ophthalmic
Marketing category
NDA AUTHORIZED GENERIC · NDA017469
Marketed since
December 15, 1994
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisolone Acetate →

Package NDC codes (3)

Package NDCDescriptionSince
61314-637-051 BOTTLE, PLASTIC in 1 CARTON (61314-637-05) / 5 mL in 1 BOTTLE, PLASTICDec 15, 1994
61314-637-101 BOTTLE, PLASTIC in 1 CARTON (61314-637-10) / 10 mL in 1 BOTTLE, PLASTICDec 15, 1994
61314-637-151 BOTTLE, PLASTIC in 1 CARTON (61314-637-15) / 15 mL in 1 BOTTLE, PLASTICDec 15, 1994

Recalls mentioning this NDC

Other Prednisolone Acetate products