NDC 53002-3401
Diphenoxylate Hydrochloride and Atropine Sulfate 2.5 mg / 0.025 mg tablet
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, 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 |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Atropine and Diphenoxylate: every company that makes it
- Form
- tablet
- Strength
- 2.5 mg / 0.025 mg
- Approval
- ANDA ANDA213413
- On the market since
- Mar 15, 2020
- Package NDCs
53002-3401-153002-3401-253002-3401-3- Official label
- DailyMed (National Library of Medicine), updated Mar 30, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?