Class II · Moderate risk
Methylphenidate hydrochloride Extended-Release ablets USP
CGMP deviations: Product bottle may be absent of desiccant.
National Drug Code
Is NDC 62037-0734-01 recalled?
Methylphenidate Hydrochloride · 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62037-734-01)
Yes — this exact package was recalled
1 FDA recall names the code 62037-0734-01 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.
- Active ingredient
- Methylphenidate Hydrochloride
- Strength
- METHYLPHENIDATE HYDROCHLORIDE 27 mg/1
- Form
- Tablet, Film Coated, Extended Release · Oral
- Labeler
- Actavis Pharma, Inc.
- Type
- Human Prescription Drug · DEA CII
- Product code
- 62037-0734
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
- 62037-0571 See recall 1
- 62037-0577 See recall 1
- 62037-0597 Cartia XT 1
- 62037-0600 Cartia XT 1
- 62037-0696 See recall 1
- 62037-0700 See recall 1
Free recall alerts
Know the day your medication is recalled
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