NDC 47335-905 – Quetiapine fumarate

Quetiapine Fumarate 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC47335-905

Product details

Brand name
Quetiapine fumarate
Generic name
Quetiapine fumarate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201190
Marketed since
March 28, 2012
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Quetiapine Fumarate →

Package NDC codes (4)

Package NDCDescriptionSince
47335-905-181000 TABLET, FILM COATED in 1 BOTTLE (47335-905-18)Mar 28, 2012
47335-905-6110 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-905-61) / 10 TABLET, FILM COATED in 1 BLISTER PACKMar 28, 2012
47335-905-8330 TABLET, FILM COATED in 1 BOTTLE (47335-905-83)Mar 28, 2012
47335-905-88100 TABLET, FILM COATED in 1 BOTTLE (47335-905-88)Mar 28, 2012

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