Class II · Moderate risk
Dr. Reddy's: Ranitidine Capsules 150 mg
CGMP Deviations: Presence of NDMA impurity detected in product.
National Drug Code
Is NDC 55111-0129-60 recalled?
Ranitidine Hydrochloride · 60 CAPSULE in 1 BOTTLE (55111-129-60)
Yes — this exact package was recalled
1 FDA recall names the code 55111-0129-60 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
- Ranitidine Hydrochloride
- Strength
- RANITIDINE HYDROCHLORIDE 150 mg/1
- Form
- Capsule · Oral
- Labeler
- Dr. Reddy's Laboratories Limited
- Type
- Human Prescription Drug
- Product code
- 55111-0129
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
- 55111-0121 Atorvastatin Calcium 4
- 55111-0123 Atorvastatin Calcium 4
- 55111-0180 Tizanidine 4
- 55111-0136 Zenatane 3
- 55111-0179 Tizanidine 3
- 55111-0320 Glimepiride 3
Free recall alerts
Know the day your medication is recalled
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