Olanzapine
- Product NDC
- 49884-323
- 11-digit product format
- 498840323
- Labeler code
- 49884
- Product ID
- 49884-323_c4415910-1493-4b5d-9723-94ae2f6c2622
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olanzapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA078109
- Marketing category
- ANDA
- Marketing start
- 2011-10-24
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 20 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 |
|---|
| 49884-323-55 | 49884032355 | 3 BLISTER PACK in 1 CARTON (49884-323-55) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-323-52) | 3 blister pack | 2011-10-24 | 0000-00-00 | No | No | Current |