Class II · Moderate risk
Fluoxetine Tablets
CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.
National Drug Code
Is NDC 13668-0473-30 recalled?
Fluoxetine · 30 TABLET in 1 BOTTLE (13668-473-30)
Yes — this exact package was recalled
1 FDA recall names the code 13668-0473-30 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
- Fluoxetine
- Strength
- FLUOXETINE HYDROCHLORIDE 20 mg/1
- Form
- Tablet · Oral
- Labeler
- Torrent Pharmaceuticals Limited
- Type
- Human Prescription Drug
- Product code
- 13668-0473
Recalls naming this package
Class II · Moderate risk
Fluoxetine Tablets
CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.
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
- 13668-0113 See recall 4
- 13668-0115 See recall 4
- 13668-0116 See recall 4
- 13668-0409 See recall 4
- 13668-0117 See recall 3
- 13668-0118 See recall 3
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