NDC 50268-549
Methenamine Hippurate 1000 mg tablet
On the label: AvPAK. It's repackaged: AvPAK rebottles it from Micro Labs Limited's NDC 42571-332.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Micro Labs Limited | Verna, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 30, 2025 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Methenamine: every company that makes it
- Form
- tablet, oral
- Strength
- 1000 mg
- Approval
- ANDA ANDA212172
- On the market since
- Dec 2, 2020
- Package NDCs
50268-549-1150268-549-15- Official label
- DailyMed (National Library of Medicine), updated Jan 9, 2024
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