NDC 0093-5377 – Clozapine

Clozapine 200 mg/1 · Tablet, Orally Disintegrating · Oral

Human Prescription Drug 1 recall

Product NDC0093-5377

Product details

Brand name
Clozapine
Generic name
Clozapine
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Orally Disintegrating
Route
Oral
Marketing category
ANDA · ANDA090308
Marketed since
July 30, 2020
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Clozapine →

Package NDC codes (2)

Package NDCDescriptionSince
0093-5377-01100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0093-5377-01)Jul 30, 2020
0093-5377-8448 BLISTER PACK in 1 CARTON (0093-5377-84) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-5377-19)Jul 30, 2020

Recalls mentioning this NDC

Other Clozapine products