Olanzapine
- Product NDC
- 50090-3267
- 11-digit product format
- 500903267
- Labeler code
- 50090
- Product ID
- 50090-3267_ac2378c7-4394-4781-8902-3e91381d5c03
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076255
- Marketing category
- ANDA
- Marketing start
- 2013-12-10
- 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