Quetiapine 76420-0522
Product NDC
76420-0522- Manufacturer
- Asclemed Usa Inc.
- 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 | 400 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(6)
100 TABLET, FILM COATED in 1 BOTTLE (76420-522-01)
10 TABLET, FILM COATED in 1 BOTTLE (76420-522-10)
20 TABLET, FILM COATED in 1 BOTTLE (76420-522-20)
30 TABLET, FILM COATED in 1 BOTTLE (76420-522-30)
60 TABLET, FILM COATED in 1 BOTTLE (76420-522-60)
90 TABLET, FILM COATED in 1 BOTTLE (76420-522-90)