NDC 72789-563
Hyoscyamine Sulfate 0.125 mg tablet, orally disintegrating
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Granulation Technology, Inc.'s NDC 63561-0197.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Granulation Technology, Inc. | Fairfield, NJ, United States | Makes it | Not inspected on record |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Hyoscyamine: every company that makes it
- Form
- tablet, orally disintegrating, oral
- Strength
- 0.125 mg
- Approval
- unapproved drug other
- On the market since
- Apr 16, 2026
- Package NDCs
72789-563-01- Official label
- DailyMed (National Library of Medicine), updated May 11, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?