NDC 0904-6805 – Quetiapine

Quetiapine Fumarate 400 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug 4 recalls

Product NDC0904-6805

Product details

Brand name
Quetiapine
Generic name
Quetiapine
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204203
Marketed since
August 22, 2017
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
0904-6805-61100 BLISTER PACK in 1 CARTON (0904-6805-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKAug 22, 2017

Recalls mentioning this NDC

Other Quetiapine products