Olanzapine
- Product NDC
- 68788-8185
- 11-digit product format
- 687888185
- Labeler code
- 68788
- Product ID
- 68788-8185_575852c8-daeb-475d-9645-454fd4fcb40b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202050
- Marketing category
- ANDA
- Marketing start
- 2022-05-06
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8185 | OLANZAPINE TABLET [PREFERRED PHARMACEUTICALS INC.] | 3 | Legacy NDC | 20240726_575852c8-daeb-475d-9645-454fd4fcb40b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8185-3 | 68788818503 | 30 TABLET in 1 BOTTLE (68788-8185-3) | 30 tablet | 2022-05-06 | 0000-00-00 | No | No | Current |
| 68788-8185-6 | 68788818506 | 60 TABLET in 1 BOTTLE (68788-8185-6) | 60 tablet | 2022-05-06 | 0000-00-00 | No | No | Current |
| 68788-8185-9 | 68788818509 | 90 TABLET in 1 BOTTLE (68788-8185-9) | 90 tablet | 2022-05-06 | 0000-00-00 | No | No | Current |