NDC 0615-8371
Trazodone Hydrochloride 50 mg tablet
On the label: NCS HealthCare of KY, Inc dba Vangard Labs. It's repackaged: NCS HealthCare of KY, Inc dba Vangard Labs rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 50111-560.
Where the pills inside were 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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- NCS HealthCare of KY, LLC dba Vangard Labs, Glasgow, KY, United States · repackages it
Recalls
- Aug 24, 2026 · Class II · Teva Pharmaceuticals USA, Inc
Presence of Foreign Tablets/Capsules
Lots: Lot: 1394026, Exp. 02/2028.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Trazodone: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA071523
- On the market since
- Oct 1, 2020
- Package NDCs
0615-8371-050615-8371-070615-8371-140615-8371-280615-8371-39- Official label
- DailyMed (National Library of Medicine), updated May 28, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?