Olanzapine
- Product NDC
- 50090-6111
- 11-digit product format
- 500906111
- Labeler code
- 50090
- Product ID
- 50090-6111_f1e98239-36cc-4e42-b4f3-003eb0bd71bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA200221
- Marketing category
- ANDA
- Marketing start
- 2012-09-13
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50090-6111-0 | 50090611100 | 28 BLISTER PACK in 1 CARTON (50090-6111-0) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 28 blister pack | 2022-09-28 | 0000-00-00 | No | No | Current |