NDC 0591-0369 – Loxapine

Loxapine Succinate 5 mg/1 · Capsule · Oral

Human Prescription Drug 3 recalls

Product NDC0591-0369

Product details

Brand name
Loxapine
Generic name
Loxapine
Labeler
Actavis Pharma, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA072204
Marketed since
June 15, 1988
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Loxapine →

Package NDC codes (1)

Package NDCDescriptionSince
0591-0369-01100 CAPSULE in 1 BOTTLE, PLASTIC (0591-0369-01)Jun 15, 1988

Recalls mentioning this NDC

Other Loxapine products