NDC 0065-8150 – Pataday Once Daily Relief

Olopatadine Hydrochloride 2 mg/mL · Solution · Ophthalmic

Human Otc Drug 1 recall

Product NDC0065-8150

Product details

Brand name
Pataday Once Daily Relief
Generic name
Olopatadine Hydrochloride
Labeler
Alcon Laboratories, Inc.
Dosage form
Solution
Route
Ophthalmic
Marketing category
NDA · NDA021545
Marketed since
February 28, 2020
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist; Histamine-1 Receptor Inhibitor; Mast Cell Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Pataday Once Daily Relief →

Package NDC codes (4)

Package NDCDescriptionSince
0065-8150-011 BOTTLE, PLASTIC in 1 CARTON (0065-8150-01) / 2.5 mL in 1 BOTTLE, PLASTICFeb 28, 2020
0065-8150-032 BOTTLE, PLASTIC in 1 CARTON (0065-8150-03) / 2.5 mL in 1 BOTTLE, PLASTICFeb 28, 2020
0065-8150-041 BOTTLE, PLASTIC in 1 CARTON (0065-8150-04) / .5 mL in 1 BOTTLE, PLASTICFeb 28, 2020
0065-8150-073 BOTTLE, PLASTIC in 1 CARTON (0065-8150-07) / 2.5 mL in 1 BOTTLE, PLASTICJan 15, 2021

Recalls mentioning this NDC

Other Pataday Once Daily Relief products