Class III ยท Low risk
buPROPion HCl Extended-Release Tablets
Failed Dissolution Specifications; during stability testing
National Drug Code
Is NDC 69097-0878-07 recalled?
Bupropion Hydrochloride (sr) · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-878-07)
Yes — this exact package was recalled
1 FDA recall names the code 69097-0878-07 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
- Bupropion Hydrochloride
- Strength
- BUPROPION HYDROCHLORIDE 150 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Cipla USA Inc.,
- Type
- Human Prescription Drug
- Product code
- 69097-0878
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
- 69097-0341 Difluprednate 3
- 69097-0410 Cinacalcet 3
- 69097-0411 Cinacalcet 3
- 69097-0412 Cinacalcet 3
- 69097-0142 Albuterol Sulfate 2
- 69097-0537 Testosterone Cypionate 2
Free recall alerts
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