Quetiapine Fumarate 47335-0906
Product NDC
47335-0906- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 28, 2012
- Listing Expires
- December 31, 2027
- Application
- ANDA201190
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Quetiapine Fumarate | 300 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(3)
10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-906-61) / 10 TABLET, FILM COATED in 1 BLISTER PACK
30 TABLET, FILM COATED in 1 BOTTLE (47335-906-83)
60 TABLET, FILM COATED in 1 BOTTLE (47335-906-86)