NDC 53002-5105
Trazodone Hydrochloride 100 mg tablet
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 50111-561.
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
- RPK Pharmaceuticals, Inc., Union City, California, 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
- Strength
- 100 mg
- Approval
- ANDA ANDA071524
- On the market since
- Oct 8, 2020
- Package NDCs
53002-5105-053002-5105-3- Official label
- DailyMed (National Library of Medicine), updated Nov 23, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?