NDC 60631-080
Edarbi 80 mg tablet
On the label: Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals).
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) names for other drugs.
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 78902-1
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Azilsartan: every company that makes it
- Form
- tablet, oral
- Strength
- 80 mg
- Approval
- NDA NDA200796
- On the market since
- Feb 1, 2013
- Package NDCs
60631-080-0760631-080-3060631-080-77- Official label
- DailyMed (National Library of Medicine), updated Jan 23, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?