Class II · Moderate risk
Alfuzosin Hydrochloride Extended-release Tablets
Presence of Foreign Substance: consumer complaint for foreign matter embedded in the tablet identified as a broken piece of wire rope from the manufacturing equipment.
National Drug Code
Is NDC 47335-0956-88 recalled?
Alfuzosin Hydrochloride · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)
Yes — this exact package was recalled
1 FDA recall names the code 47335-0956-88 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
- Alfuzosin Hydrochloride
- Strength
- ALFUZOSIN HYDROCHLORIDE 10 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 47335-0956
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
- 47335-0737 Bupropion hydrochloride 6
- 47335-0738 Bupropion hydrochloride 5
- 47335-0506 Cequa 4
- 47335-0063 Dofetilide 2
- 47335-0343 See recall 2
- 47335-0049 Doxorubicin Hydrochloride 1
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