NDC 70518-4555
Dicyclomine hydrochloride 20 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-079.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Annora Pharma Private Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilyMar 28, 2025 · 4 inspections |
Product details
- Generic drug
- Dicyclomine: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA217566
- On the market since
- Jan 26, 2026
- Package NDCs
70518-4555-0- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2026
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