Quetiapine 33342-0135
Product NDC
33342-0135- Manufacturer
- Macleods Pharmaceuticals Limited
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 1, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA204253
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Quetiapine Fumarate | 200 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(2)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-135-09)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-135-15)