NDC 43598-165 – Olanzapine

Olanzapine 7.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC43598-165

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 (5)

Package NDCDescriptionSince
43598-165-01100 TABLET, FILM COATED in 1 BOTTLE (43598-165-01)Dec 10, 2013
43598-165-05500 TABLET, FILM COATED in 1 BOTTLE (43598-165-05)Dec 10, 2013
43598-165-3030 TABLET, FILM COATED in 1 BOTTLE (43598-165-30)Dec 10, 2013
43598-165-6060 TABLET, FILM COATED in 1 BOTTLE (43598-165-60)Dec 10, 2013
43598-165-7810 BLISTER PACK in 1 CARTON (43598-165-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-165-79)Dec 10, 2013

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