Class III · Low risk
Benzphetamine tablets
Labeling: Label Mix-up: Bottle labeled as Benzonatate 100 mg capsules contained Benzphetamine 50 mg tablets and a bottle labeled as Benzphetamine 50 mg tablets contained Benzonatate 100 mg capsules.
National Drug Code
Is NDC 10702-0040-50 recalled?
Benzphetamine Hydrochloride · 500 TABLET in 1 BOTTLE (10702-040-50)
Yes — this exact package was recalled
1 FDA recall names the code 10702-0040-50 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
- benzphetamine hydrochloride
- Strength
- BENZPHETAMINE HYDROCHLORIDE 50 mg/1
- Form
- Tablet · Oral
- Labeler
- Kvk-Tech, INC
- Type
- Human Prescription Drug · DEA CIII
- Product code
- 10702-0040
Recalls naming this package
Class III · Low risk
Benzphetamine Hydrochloride Tablets
Discoloration: presence of scuffing marks on tablets.
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
- 10702-0028 Phentermine 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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