Olanzapine
- Product NDC
- 50090-4040
- 11-digit product format
- 500904040
- Labeler code
- 50090
- Product ID
- 50090-4040_396f0ca9-cd21-45fc-b978-129e30e346fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204319
- Marketing category
- ANDA
- Marketing start
- 2018-01-19
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50090-4040-0 | 50090404000 | 1 BOX, UNIT-DOSE in 1 BLISTER PACK (50090-4040-0) > 33 TABLET in 1 BOX, UNIT-DOSE | 2019-01-10 | 0000-00-00 | No | No | Current |