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

Is NDC 70010-0231-01 recalled?

Trazodone Hydrochloride · 100 TABLET in 1 BOTTLE (70010-231-01)

Yes — this exact package was recalled

1 FDA recall names the code 70010-0231-01 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
Trazodone Hydrochloride
Strength
TRAZODONE HYDROCHLORIDE 50 mg/1
Form
Tablet · Oral
Labeler
Granules Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
70010-0231

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

  • 70010-0001 Colchicine 1
  • 70010-0029 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1
  • 70010-0030 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1
  • 70010-0031 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1
  • 70010-0032 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1
  • 70010-0034 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1