Class III ยท Low risk
Pred Mild
Failed Stability Specifications
National Drug Code
Is NDC 11980-0174-10 recalled?
Pred Mild · 1 BOTTLE, DROPPER in 1 CARTON (11980-174-10) / 10 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
1 FDA recall names the code 11980-0174-10 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
- prednisolone acetate
- Strength
- PREDNISOLONE ACETATE 1.2 mg/mL
- Form
- Suspension/ Drops · Ophthalmic
- Labeler
- Allergan, Inc.
- Type
- Human Prescription Drug
- Product code
- 11980-0174
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.
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