NDC 70518-3915
Diphenoxylate Hydrochloride and Atropine Sulfate 2.5 mg / 0.025 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Leading Pharma, LLC's NDC 69315-910.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Leading Pharma, LLC | Fairfield, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyOct 21, 2024 · 13 inspections |
Product details
- Generic drug
- Atropine and Diphenoxylate: every company that makes it
- Form
- tablet, oral
- Strength
- 2.5 mg / 0.025 mg
- Approval
- ANDA ANDA213413
- On the market since
- Nov 16, 2023
- Package NDCs
70518-3915-070518-3915-1- Official label
- DailyMed (National Library of Medicine), updated Jun 10, 2026
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