Class II ยท Moderate risk
Bisacodyl Suppositories
CGMP Deviations: products were stored outside the drug label specifications.
National Drug Code
Is NDC 57896-0443-01 recalled?
Bisacodyl · 20 BLISTER PACK in 1 CARTON (57896-443-01) / 5 SUPPOSITORY in 1 BLISTER PACK (57896-443-55)
Yes — this exact package was recalled
1 FDA recall names the code 57896-0443-01 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
- Bisacodyl
- Strength
- BISACODYL 10 mg/1
- Form
- Suppository · Rectal
- Labeler
- Geri-Care Pharmaceutical CORP
- Type
- Human OTC Drug
- Product code
- 57896-0443
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
- 57896-0181 Artificial Tears 2
- 57896-0403 See recall 2
- 57896-0709 See recall 2
- 57896-0186 See recall 1
- 57896-0401 Stool Softener 1
- 57896-0660 See recall 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.