Olanzapine
- Product NDC
- 63629-8274
- 11-digit product format
- 636298274
- Labeler code
- 63629
- Product ID
- 63629-8274_8a57ee71-3bf8-4edc-bb36-8ef00a6b1a26
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202862
- Marketing category
- ANDA
- Marketing start
- 2014-08-22
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 15 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 |
|---|
| 63629-8274-1 | 63629827401 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8274-1) | 2019-11-27 | 0000-00-00 | No | No | Current |