Olanzapine
- Product NDC
- 70518-1207
- 11-digit product format
- 705181207
- Labeler code
- 70518
- Product ID
- 70518-1207_909d974e-7315-bddb-e053-2995a90a06bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091265
- Marketing category
- ANDA
- Marketing start
- 2018-05-15
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record