Zyprexa
- Product NDC
- 49999-606
- 11-digit product format
- 499990606
- Labeler code
- 49999
- Product ID
- 49999-606_22ed737e-df95-4780-bf50-5f53ef9887d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- NDA020592
- Marketing category
- NDA
- Marketing start
- 2012-03-30
- 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