NDC 50268-652
Pilocarpine Hydrochloride 5 mg tablet, film coated
On the label: AvPAK. It's repackaged: AvPAK rebottles it from Lannett Company, Inc.'s NDC 0527-1313.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Pilocarpine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA077220
- On the market since
- Jan 7, 2021
- Package NDCs
50268-652-1150268-652-12- Official label
- DailyMed (National Library of Medicine), updated Nov 15, 2022
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