Class II ยท Moderate risk
Metoprolol Tartrate and Hydrochlorothiazide Tablets
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 62332-0115-31 recalled?
Metoprolol Tartrate and Hydrochlorothiazide · 100 TABLET in 1 BOTTLE (62332-115-31)
Yes — this exact package was recalled
1 FDA recall names the code 62332-0115-31 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
- Metoprolol Tartrate and Hydrochlorothiazide
- Strength
- METOPROLOL TARTRATE 50 mg/1; HYDROCHLOROTHIAZIDE 25 mg/1
- Form
- Tablet · Oral
- Labeler
- Alembic Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 62332-0115
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
- 62332-0508 Bromfenac Ophthalmic Solution 0.09% 2
- 62332-0087 Telmisartan 1
- 62332-0097 Aripiprazole 1
- 62332-0142 Celecoxib 1
- 62332-0175 Fesoterodine Fumarate 1
- 62332-0176 Fesoterodine Fumarate 1
Free recall alerts
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