Olanzapine
- Product NDC
- 55700-862
- 11-digit product format
- 557000862
- Labeler code
- 55700
- Product ID
- 55700-862_597525e7-70d7-428b-a7be-091730191e0b
- 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
- 2020-05-15
- 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 |
|---|
| 55700-862-30 | 55700086230 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-862-30) | 2020-05-15 | 0000-00-00 | No | No | Current |