Class II · Moderate risk
Methylphenidate Hydrochloride
Failed dissolution specifications: this product is being recalled due to this batch not meeting dissolution specifications.
National Drug Code
Is NDC 13811-0708-10 recalled?
Methylphenidate Hydrochloride · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-708-10)
Yes — this exact package was recalled
2 FDA recalls name the code 13811-0708-10 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
- Methylphenidate hydrochloride
- Strength
- METHYLPHENIDATE HYDROCHLORIDE 36 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Trigen Laboratories, LLC
- Type
- Human Prescription Drug · DEA CII
- Product code
- 13811-0708
Recalls naming this package
Class III · Low risk
Methylphenidate Hydrochloride Extended-release Tablets
Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL ER Tablets 36 mg found to contain 1 27 mg Methylphenidate HCL ER Tablet.
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
- 13811-0001 See recall 1
- 13811-0002 See recall 1
- 13811-0067 See recall 1
- 13811-0068 See recall 1
- 13811-0071 See recall 1
- 13811-0072 See recall 1
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