Class II · Moderate risk
Phendimetrazine Yellow Tabs 35mg
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
National Drug Code
Is NDC 69543-0410-11 recalled?
Phendimetrazine Tartrate · 1000 TABLET in 1 BOTTLE (69543-410-11)
Yes — this exact package was recalled
1 FDA recall names the code 69543-0410-11 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
- Phendimetrazine Tartrate
- Strength
- PHENDIMETRAZINE TARTRATE 35 mg/1
- Form
- Tablet · Oral
- Labeler
- Virtus Pharmaceuticals, LLC
- Type
- Human Prescription Drug · DEA CIII
- Product code
- 69543-0410
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
- 69543-0224 See recall 2
- 69543-0409 See recall 1
Free recall alerts
Know the day your medication is recalled
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