Olanzapine
- Product NDC
- 27241-077
- 11-digit product format
- 272410077
- Labeler code
- 27241
- Product ID
- 27241-077_288c8fdc-78c0-4fb3-b19a-063732ae5093
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ajanta Pharma Limited
- Application
- ANDA206711
- Marketing category
- ANDA
- Marketing start
- 2017-03-16
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record