Class II · Moderate risk
Chlorthalidone Tablets USP 25 mg
Foreign Matter identified as stainless steel microscopic wear particles mixed with punch lubricant oil and silicone particles from the dust cup
National Drug Code
Is NDC 57664-0648-88 recalled?
Chlorthalidone · 100 TABLET in 1 BOTTLE (57664-648-88)
Yes — this exact package was recalled
1 FDA recall names the code 57664-0648-88 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
- Chlorthalidone
- Strength
- CHLORTHALIDONE 25 mg/1
- Form
- Tablet · Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 57664-0648
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
- 57664-0051 Lisdexamfetamine Dimesylate 2
- 57664-0135 See recall 2
- 57664-0377 See recall 2
- 57664-0506 See recall 2
- 57664-0783 See recall 2
- 57664-0046 Lisdexamfetamine Dimesylate 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.