OLANZAPINE
- Product NDC
- 35573-426
- 11-digit product format
- 355730426
- Labeler code
- 35573
- Product ID
- 35573-426_eda6b4a9-342f-4efa-b002-79ce056d4219
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Burel Pharmaceuticals, LLC
- Application
- ANDA202050
- Marketing category
- ANDA
- Marketing start
- 2012-04-23
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35573-426-30 | 35573042630 | 30 TABLET in 1 BOTTLE (35573-426-30) | 30 tablet | 2012-04-23 | 0000-00-00 | No | No | Current |