NDC 71205-568
Trazodone Hydrochloride 50 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP 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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels 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
71205-568-3071205-568-6071205-568-90- Official label
- DailyMed (National Library of Medicine), updated Jun 1, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?