NDC 0093-8166 – Quetiapine

Quetiapine Fumarate 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0093-8166

Product details

Brand name
Quetiapine
Generic name
Quetiapine
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077745
Marketed since
March 27, 2012
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Quetiapine →

Package NDC codes (1)

Package NDCDescriptionSince
0093-8166-01100 TABLET, FILM COATED in 1 BOTTLE (0093-8166-01)Mar 27, 2012

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