Olanzapine
- Product NDC
- 70518-2623
- 11-digit product format
- 705182623
- Labeler code
- 70518
- Product ID
- 70518-2623_caf45a44-8ac1-292a-e053-2a95a90a197f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204319
- Marketing category
- ANDA
- Marketing start
- 2020-03-10
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 20 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 |
|---|
| 70518-2623-0 | 70518262300 | 30 TABLET in 1 BLISTER PACK (70518-2623-0) | 30 tablet | 2020-03-10 | 0000-00-00 | No | No | Current |