NDC 50268-522
Meclizine Hydrochloride 12.5 mg tablet
On the label: AvPAK. It's repackaged: AvPAK rebottles it from Amneal Pharmaceuticals's NDC 53746-441.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals Private Limited | Ahmedabad, India | Makes it, tests it, packages it and labels it | No problems foundJul 19, 2024 · 6 inspections |
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Meclizine: every company that makes it
- Form
- tablet, oral
- Strength
- 12.5 mg
- Approval
- ANDA ANDA201451
- On the market since
- Aug 8, 2013
- Package NDCs
50268-522-1150268-522-15- Official label
- DailyMed (National Library of Medicine), updated Oct 26, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?