NDC 70518-0921 – Olanzapine

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

Human Prescription Drug

Product NDC70518-0921

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202862
Marketed since
December 26, 2017
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine →

Package NDC codes (1)

Package NDCDescriptionSince
70518-0921-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-0921-0)Dec 26, 2017

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