Class II ยท Moderate risk
Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules, USP)
Labelling: Incorrect Exp. Date
National Drug Code
Is NDC 62037-0597-90 recalled?
Cartia XT · 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-597-90)
Yes — this exact package was recalled
1 FDA recall names the code 62037-0597-90 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
- Diltiazem Hydrochloride
- Strength
- DILTIAZEM HYDROCHLORIDE 120 mg/1
- Form
- Capsule, Extended Release · Oral
- Labeler
- Actavis Pharma, Inc.
- Type
- Human Prescription Drug
- Product code
- 62037-0597
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
- 62037-0600 Cartia XT 1
- 62037-0696 See recall 1
- 62037-0700 See recall 1
- 62037-0725 Methylphenidate Hydrochloride 1
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