NDC 0781-6206 – Bimatoprost

Bimatoprost .3 mg/mL · Solution/ Drops · Ophthalmic

Human Prescription Drug 1 recall

Product NDC0781-6206

Product details

Brand name
Bimatoprost
Generic name
Bimatoprost
Labeler
Sandoz Inc
Dosage form
Solution/ Drops
Route
Ophthalmic
Marketing category
ANDA · ANDA202719
Marketed since
December 6, 2016
Listing expires
December 31, 2026
Pharmacologic class
Prostaglandin Analog

Active ingredients

Uses, dosage, side effects and warnings for Bimatoprost →

Package NDC codes (2)

Package NDCDescriptionSince
0781-6206-751 BOTTLE, WITH APPLICATOR in 1 CARTON (0781-6206-75) / 5 mL in 1 BOTTLE, WITH APPLICATORDec 6, 2016
0781-6206-931 BOTTLE, WITH APPLICATOR in 1 CARTON (0781-6206-93) / 3 mL in 1 BOTTLE, WITH APPLICATORDec 6, 2016

Recalls mentioning this NDC

Other Bimatoprost products