NDC 43598-166 – Olanzapine

Olanzapine 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC43598-166

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
Dr. Reddy's Laboratories Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076255
Marketed since
December 10, 2013
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine →

Package NDC codes (6)

Package NDCDescriptionSince
43598-166-01100 TABLET, FILM COATED in 1 BOTTLE (43598-166-01)Dec 10, 2013
43598-166-05500 TABLET, FILM COATED in 1 BOTTLE (43598-166-05)Dec 10, 2013
43598-166-101000 TABLET, FILM COATED in 1 BOTTLE (43598-166-10)Dec 10, 2013
43598-166-3030 TABLET, FILM COATED in 1 BOTTLE (43598-166-30)Dec 10, 2013
43598-166-6060 TABLET, FILM COATED in 1 BOTTLE (43598-166-60)Dec 10, 2013
43598-166-7810 BLISTER PACK in 1 CARTON (43598-166-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-166-79)Dec 10, 2013

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