Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 10702-0026-10 recalled?

Phentermine Hydrochloride · 1000 CAPSULE in 1 BOTTLE (10702-026-10)

Yes — this exact package was recalled

3 FDA recalls name the code 10702-0026-10 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
KVK-Tech, Inc.
Type
Human Prescription Drug · DEA CIV
Product code
10702-0026

Recalls naming this package

Class II · Moderate risk

Phentermine HCL Gray/Yellow capsules

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Terminated cGMP deviation Calvin Scott & Company, Inc. NDC 10702-0026-10 D-1524-2020
Class III · Low risk

Phentermine HCL Capsules

Failed Impurities/Degradation Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature Retained Sample stability test.

Terminated Impurity / degradation KVK-Tech, Inc. NDC 10702-026-01 D-1083-2017
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

Terminated Impurity / degradation KVK-Tech, Inc. NDC 10702-0026-01 D-1371-2015

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