Quetiapine 67877-0242
Product NDC
67877-0242- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 1, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA201504
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Quetiapine Fumarate | 25 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (67877-242-01)
1000 TABLET, FILM COATED in 1 BOTTLE (67877-242-10)
1 BLISTER PACK in 1 CARTON (67877-242-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK
10 BLISTER PACK in 1 CARTON (67877-242-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK