Olanzapine
- Product NDC
- 55700-809
- 11-digit product format
- 557000809
- Labeler code
- 55700
- Product ID
- 55700-809_6b4b0802-096f-4102-a072-398052a73fe5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA202862
- Marketing category
- ANDA
- Marketing start
- 2019-10-18
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 55700-809-30 | 55700080930 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-809-30) | 2019-10-18 | 0000-00-00 | No | No | Current |