NDC 33261-163
Dicyclomine Hydrochloride 20 mg tablet
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC rebottles it from Lannett Company, Inc.'s NDC 0527-1282.
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
- Dicyclomine: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA040230
- On the market since
- Feb 26, 1999
- Package NDCs
33261-163-0233261-163-3033261-163-6033261-163-90- Official label
- DailyMed (National Library of Medicine), updated Dec 27, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?