NDC 0093-5377
Clozapine 200 mg tablet, orally disintegrating
On the label: Teva Pharmaceuticals USA, Inc..
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Recalls
- Sep 21, 2018 · Class II · Teva Pharmaceuticals USA
Failed Disintegration Specifications: Out-of-specification disintegration test result obtained during routine stability testing.
Lots: Lot #: 34034024B, Exp 02/20
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Clozapine: every company that makes it
- Form
- tablet, orally disintegrating, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA090308
- On the market since
- Jul 30, 2020
- Package NDCs
0093-5377-010093-5377-190093-5377-84- Official label
- DailyMed (National Library of Medicine), updated Jun 24, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?