Olanzapine
- Product NDC
- 63629-2237
- 11-digit product format
- 636292237
- Labeler code
- 63629
- Product ID
- 63629-2237_42bb57c4-7d36-423a-9728-dcad67caca71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078109
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2237-1 | 63629223701 | 3 BLISTER PACK in 1 CARTON (63629-2237-1) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 3 blister pack | 2011-10-24 | 0000-00-00 | No | No | Current |