Olanzapine
- Product NDC
- 48792-7858
- 11-digit product format
- 487927858
- Labeler code
- 48792
- Product ID
- 48792-7858_70a02281-2685-1588-e053-2991aa0ae09e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Sunshine Lake Pharma Co., Ltd.
- Application
- ANDA208146
- Marketing category
- ANDA
- Marketing start
- 2018-07-10
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48792-7858-1 | 48792785801 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (48792-7858-1) | 2018-07-10 | 0000-00-00 | No | No | Current |