NDC 70518-4331
Dicyclomine Hydrochloride 10 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-719.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
Recalls
- Jul 23, 2026 · Class II · Aurobindo Pharma USA Inc
shortfill; reports of empty capsules.
Lots: Batch # DMC125018A, Exp Date: 07/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Dicyclomine: every company that makes it
- Form
- capsule, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA040319
- On the market since
- Apr 19, 2025
- Package NDCs
70518-4331-070518-4331-1- Official label
- DailyMed (National Library of Medicine), updated Sep 4, 2026
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