Class II · Moderate risk
Dorzolamide HCl and Timolol Maleate Ophthalmic Solution
Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.
National Drug Code
Is NDC 42571-0147-26 recalled?
Dorzolamide Hydrochloride and Timolol Maleate ophthalmic Solution · 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 42571-0147-26 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
- Dorzolamide Hydrochloride and Timolol Maleate
- Strength
- DORZOLAMIDE HYDROCHLORIDE 22.3 mg/mL; TIMOLOL MALEATE 6.8…
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Micro Labs Limited
- Type
- Human Prescription Drug
- Product code
- 42571-0147
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
- 42571-0010 See recall 1
- 42571-0020 See recall 1
- 42571-0040 See recall 1
- 42571-0080 See recall 1
- 42571-0101 Glimepiride 1
- 42571-0110 See recall 1
Free recall alerts
Know the day your medication is recalled
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