Olanzapine
- Product NDC
- 63629-7514
- 11-digit product format
- 636297514
- Labeler code
- 63629
- Product ID
- 63629-7514_02d44200-1c7e-419b-bfa9-68ead51ec379
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7514-1 | 63629751401 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-7514-1) | 2018-01-29 | 0000-00-00 | No | No | Current |
| 63629-7514-2 | 63629751402 | 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-7514-2) | 2018-01-29 | 0000-00-00 | No | No | Current |
| 63629-7514-3 | 63629751403 | 60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-7514-3) | 2018-01-29 | 0000-00-00 | No | No | Current |