Class II · Moderate risk
Phentermine Hydrochloride Capsules
cGMP deviations
National Drug Code
Is NDC 10702-0028-01 recalled?
Phentermine Hydrochloride · 100 CAPSULE in 1 BOTTLE (10702-028-01)
Yes — this exact package was recalled
1 FDA recall names the code 10702-0028-01 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
- Phentermine Hydrochloride
- Strength
- PHENTERMINE HYDROCHLORIDE 30 mg/1
- Form
- Capsule · Oral
- Labeler
- KVK-Tech, Inc.
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 10702-0028
Recalls naming this package
Class II · Moderate risk
Phentermine HCL Blue/Clear capsules
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
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
- 10702-0026 Phentermine Hydrochloride 3
- 10702-0040 Benzphetamine Hydrochloride 2
- 10702-0052 See recall 2
- 10702-0010 Hydroxyzine Hydrochloride 1
- 10702-0011 Hydroxyzine Hydrochloride 1
- 10702-0012 Hydroxyzine Hydrochloride 1
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