Class II · Moderate risk
Albuterol 0.083% Inh Sol. 30 days supply
Lack of Processing Controls.
National Drug Code
Is NDC 76204-0200-60 recalled?
Albuterol Sulfate · 2 POUCH in 1 CARTON (76204-200-60) / 30 AMPULE in 1 POUCH / 3 mL in 1 AMPULE
Yes — this exact package was recalled
1 FDA recall names the code 76204-0200-60 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.
- Active ingredient
- Albuterol Sulfate
- Strength
- ALBUTEROL SULFATE 2.5 mg/3mL
- Form
- Solution · Respiratory (inhalation)
- Labeler
- Ritedose Pharmaceuticals, LLC
- Type
- Human Prescription Drug
- Product code
- 76204-0200
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
- 76204-0025 See recall 1
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