Class II · Moderate risk
Bromfenac Ophthalmic Solution 0.07%
Failed Impurities/Degradation Specifications: out of specification at the time of testing i.e. 20th month stability testing.
National Drug Code
Is NDC 62332-0583-03 recalled?
Bromfenac Sodium · 1 BOTTLE in 1 CARTON (62332-583-03) / 3 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 62332-0583-03 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Bromfenac Sodium
- Strength
- BROMFENAC SODIUM .805 mg/mL
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Alembic Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 62332-0583
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 62332-0508 Bromfenac Ophthalmic Solution 0.09% 2
- 62332-0087 Telmisartan 1
- 62332-0097 Aripiprazole 1
- 62332-0115 Metoprolol Tartrate and Hydrochlorothiazide 1
- 62332-0142 Celecoxib 1
- 62332-0175 Fesoterodine Fumarate 1
Free recall alerts
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