Olanzapine
- Product NDC
- 71335-0663
- 11-digit product format
- 713350663
- Labeler code
- 71335
- Product ID
- 71335-0663_b1ec5023-b921-42af-9e0e-81f45271d966
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076534
- Marketing category
- ANDA
- Marketing start
- 2011-10-24
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0663-1 | 71335066301 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0663-1) | 2018-01-29 | 0000-00-00 | No | No | Current |
| 71335-0663-2 | 71335066302 | 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0663-2) | 2018-01-29 | 0000-00-00 | No | No | Current |
| 71335-0663-3 | 71335066303 | 60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0663-3) | 2018-01-29 | 0000-00-00 | No | No | Current |