NDC 70518-3917
Dicyclomine Hydrochloride 20 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 24979-200.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceutical Laboratories Inc. | Zhunan Township, Taiwan | Makes it, tests it and packages it | Problems found, fixed voluntarilyJul 21, 2025 · 7 inspections |
| Bora Pharmaceutical Laboratories Inc. Zhongli Plant | Taoyuan City, Taiwan | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 7, 2020 · 4 inspections |
Product details
- Generic drug
- Dicyclomine: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA216782
- On the market since
- Nov 19, 2023
- Package NDCs
70518-3917-070518-3917-170518-3917-270518-3917-370518-3917-470518-3917-5- Official label
- DailyMed (National Library of Medicine), updated Aug 18, 2026
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