Class III · Low risk
Brimonidine Tartrate Opthalmic Solution 0.2%
Failed Impurities/Degradation Specification: There is a slow leaching process from the product label on the bottle which may impact the product over the shelf life.
National Drug Code
Is NDC 70069-0233-01 recalled?
Brimonidine Tartrate · 1 BOTTLE in 1 CARTON (70069-233-01) / 15 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 70069-0233-01 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.
- Active ingredient
- Brimonidine Tartrate
- Strength
- BRIMONIDINE TARTRATE 2 mg/mL
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Somerset Therapeutics, LLC
- Type
- Human Prescription Drug
- Product code
- 70069-0233
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
- 70069-0381 Haloperidol Decanoate 2
- 70069-0025 Dexamethasone Sodium Phosphate 1
- 70069-0101 Methocarbamol 1
- 70069-0141 Cisatracurium Besylate 1
- 70069-0151 Cisatracurium Besylate 1
- 70069-0161 Cisatracurium Besylate 1
Free recall alerts
Know the day your medication is recalled
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