Aurobindo recalls dicyclomine 10mg capsules over underfilled bottles and reports of empty capsules
Some 1,000-count bottles of dicyclomine hydrochloride 10mg capsules were not filled to the right amount, and there have been reports of empty capsules.
What to do
The notice does not give instructions. Read the official notice for details.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Recall details
- Product
- Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India, NDC 59651-719-99
- Company
- Aurobindo Pharma USA Inc
- Hazard
- shortfill; reports of empty capsules.
- Units
- 6,408 bottles distributed to market
- Where sold
- US Nationwide.
- FDA classification
- Class II · Ongoing
- Classified by FDA
- August 4, 2026
- Recall started
- July 23, 2026
- FDA enforcement report
- August 12, 2026
- Identifiers
- Codes: Batch # DMC125018A, Exp Date: 07/2027.
- FDA recall number: D-0733-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- Product
- Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India, NDC 59651-719-99
- Reason for recall
- shortfill; reports of empty capsules.
- Classification
- Class II (Ongoing)
- Distribution
- US Nationwide.
- Quantity
- 6,408 bottles distributed to market
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