Olanzapine
- Product NDC
- 55154-5877
- 11-digit product format
- 551545877
- Labeler code
- 55154
- Product ID
- 55154-5877_a3c8fd94-4abf-406f-98da-f44fb6a8498a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076255
- Marketing category
- ANDA
- Marketing start
- 2012-04-23
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record