NDC 70069-431
Dicyclomine Hydrochloride 10 mg per 1 mL injection, solution
On the label: Somerset Therapeutics, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Somerset Therapeutics Private Limited | Bengaluru, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 21, 2025 · 10 inspections, 4 with FDA action |
Product details
- Generic drug
- Dicyclomine: every company that makes it
- Form
- injection, solution, intramuscular
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA214332
- On the market since
- Nov 5, 2024
- Package NDCs
70069-431-0170069-431-05- Official label
- DailyMed (National Library of Medicine), updated Nov 5, 2024
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