Olanzapine
- Product NDC
- 50090-3967
- 11-digit product format
- 500903967
- Labeler code
- 50090
- Product ID
- 50090-3967_728b0c7d-155b-43e1-87d5-f90bcadb74e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078109
- Marketing category
- ANDA
- Marketing start
- 2011-10-24
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3967-0 | Olanzapine | 10 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 10 | | 6 |
| 50090-3967-0 | Olanzapine | 3 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 3 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3967 | OLANZAPINE TABLET, ORALLY DISINTEGRATING [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 2 package rows | 20210617_3aa5007a-8547-4991-a51d-59829837ac61.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3967-0 | 50090396700 | 3 BLISTER PACK in 1 CARTON (50090-3967-0) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 3 blister pack | 2018-12-13 | 0000-00-00 | No | No | Current |