Clozapine
- Product NDC
- 0781-5989
- 11-digit product format
- 007815989
- Labeler code
- 0781
- Product ID
- 0781-5989_9da402bb-c2b6-4db2-af7c-90e5c3d6f35c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clozapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc.
- Application
- NDA019758
- Marketing category
- NDA
- Marketing start
- 2016-05-06
- Marketing end
- 2021-06-30
- Substance
- CLOZAPINE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0781-5989-01 | 00781598901 | 100 TABLET in 1 BOTTLE (0781-5989-01) | 100 tablet | 2016-05-06 | 2021-06-30 | No | No | Current |