NDC 67877-250 – Quetiapine

Quetiapine Fumarate 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC67877-250

Product details

Brand name
Quetiapine
Generic name
Quetiapine
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201504
Marketed since
March 1, 2013
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Quetiapine →

Package NDC codes (4)

Package NDCDescriptionSince
67877-250-01100 TABLET, FILM COATED in 1 BOTTLE (67877-250-01)Mar 1, 2013
67877-250-101000 TABLET, FILM COATED in 1 BOTTLE (67877-250-10)Mar 1, 2013
67877-250-331 BLISTER PACK in 1 CARTON (67877-250-33) / 10 TABLET, FILM COATED in 1 BLISTER PACKMar 1, 2013
67877-250-3810 BLISTER PACK in 1 CARTON (67877-250-38) / 10 TABLET, FILM COATED in 1 BLISTER PACKMar 1, 2013

Recalls mentioning this NDC

Other Quetiapine products