Class II · Moderate risk
buPROPion Hydrochloride Extended-Release Tablets
Presence of Foreign Tablets/Capsules
National Drug Code
Is NDC 16571-0862-03 recalled?
bupropion hydrochloride · 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-862-03)
Yes — this exact package was recalled
1 FDA recall names the code 16571-0862-03 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.
1 of these recalls is still ongoing.
- Active ingredient
- bupropion hydrochloride
- Strength
- BUPROPION HYDROCHLORIDE 150 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Rising Pharma Holdings, Inc.
- Type
- Human Prescription Drug
- Product code
- 16571-0862
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
- 16571-0130 See recall 2
- 16571-0140 See recall 2
- 16571-0141 See recall 2
- 16571-0402 Cetirizine Hydrochloride 2
- 16571-0742 See recall 2
- 16571-0301 See recall 1
Free recall alerts
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