NDC 43063-741
Methscopolamine Bromide 5 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 76385-101.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sunrise Pharmaceutical Inc | Rahway, NJ, United States | Makes it | Problems found, fixed voluntarilyMar 31, 2026 · 8 inspections, 1 with FDA action |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Methscopolamine: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA200602
- On the market since
- Oct 1, 2013
- Package NDCs
43063-741-60- Official label
- DailyMed (National Library of Medicine), updated Jan 5, 2026
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