NDC 71205-904
Midodrine Hydrochloride 2.5 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Xiromed, LLC.'s NDC 70700-157.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cerovene, Inc. | Valley Cottage, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMar 23, 2026 · 9 inspections |
| Nutra-Med Packaging LLC | Whippany, NJ, United States | Packages it | No problems foundNov 20, 2024 · 6 inspections |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Midodrine: every company that makes it
- Form
- tablet, oral
- Strength
- 2.5 mg
- Approval
- ANDA ANDA207849
- On the market since
- Oct 15, 2020
- Package NDCs
71205-904-0071205-904-1171205-904-3071205-904-5571205-904-6071205-904-7271205-904-90- Official label
- DailyMed (National Library of Medicine), updated Apr 1, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?