Class III · Low risk
Atropine Sulfate Ophthalmic Solution
Failed Impurities/Degradation Specifications
National Drug Code
Is NDC 70069-0716-01 recalled?
Atropine Sulfate · 1 BOTTLE in 1 CARTON (70069-716-01) / 5 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 70069-0716-01 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
- Atropine Sulfate Monohydrate
- Strength
- ATROPINE SULFATE 10 mg/mL
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Somerset Therapeutics, LLC
- Type
- Human Prescription Drug
- Product code
- 70069-0716
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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