NDC 68071-2822
Trazodone Hydrochloride 50 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. 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
- NuCare Pharmaceuticals,Inc., Orange, CA, 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
- Strength
- 50 mg
- Approval
- ANDA ANDA071523
- On the market since
- Oct 1, 2020
- Package NDCs
68071-2822-3- Official label
- DailyMed (National Library of Medicine), updated Aug 30, 2022
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