Olanzapine
- Product NDC
- 72789-265
- 11-digit product format
- 727890265
- Labeler code
- 72789
- Product ID
- 72789-265_e662f761-f1b9-0de8-e053-2a95a90a9d13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA091265
- 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
- 2023-12-31
- 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 |
|---|
| 72789-265-03 | 72789026503 | 3 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (72789-265-03) | 2022-08-16 | 0000-00-00 | No | No | Current |