Class III · Low risk
Phentermine Capsules
Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at 30th month Room Temperature Retained Sample stabilities test .
National Drug Code
Is NDC 55289-0791-21 recalled?
Phentermine Hydrochloride · 21 CAPSULE in 1 BOTTLE, PLASTIC (55289-791-21)
Yes — this exact package was recalled
1 FDA recall names the code 55289-0791-21 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
- Phentermine Hydrochloride
- Strength
- PHENTERMINE HYDROCHLORIDE 15 mg/1
- Form
- Capsule · Oral
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 55289-0791
Recalls naming this package
Class III · Low risk
Phentermine Hydrochloride Capsules
Failed impurities/Degradation specifications: out of specification results for individual unknown and total impurity at the 12th month room temperature stability test station
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
- 55289-0866 Doxycycline 2
- 55289-0274 See recall 1
- 55289-0673 See recall 1
- 55289-0765 See recall 1
- 55289-0964 See recall 1
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