Olanzapine
- Product NDC
- 63187-329
- 11-digit product format
- 631870329
- Labeler code
- 63187
- Product ID
- 63187-329_2871d405-e727-4ef1-9857-69cd83accdc4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076133
- Marketing category
- ANDA
- Marketing start
- 2011-10-24
- 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