Olanzapine
- Product NDC
- 50090-3405
- 11-digit product format
- 500903405
- Labeler code
- 50090
- Product ID
- 50090-3405_bbba22c5-8263-4c09-a0f9-1c9062876519
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091265
- Marketing category
- ANDA
- Marketing start
- 2011-10-24
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record