Class III · Low risk
Albuterol Sulfate
Failed Stability Specifications: Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the 12-month time point.
National Drug Code
Is NDC 69097-0142-60 recalled?
Albuterol Sulfate · 1 CANISTER in 1 CARTON (69097-142-60) / 200 INHALANT in 1 CANISTER
Yes — this exact package was recalled
2 FDA recalls name the code 69097-0142-60 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
- albuterol sulfate
- Strength
- ALBUTEROL SULFATE 90 ug/1
- Form
- Inhalant · Respiratory (inhalation)
- Labeler
- Cipla USA Inc.
- Type
- Human Prescription Drug
- Product code
- 69097-0142
Recalls naming this package
Class I · High risk
Albuterol Sulfate Inhalation Aerosol
Defective container: empty inhaler and leakage observed through the inhaler valve due to partially missing bottom seat (gasket).
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
- 69097-0341 Difluprednate 3
- 69097-0410 Cinacalcet 3
- 69097-0411 Cinacalcet 3
- 69097-0412 Cinacalcet 3
- 69097-0537 Testosterone Cypionate 2
- 69097-0870 Lanreotide Acetate 2
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