Clozapine
- Product NDC
- 51862-274
- 11-digit product format
- 518620274
- Labeler code
- 51862
- Product ID
- 51862-274_e3477b46-cdcf-4c25-b43e-3cdce74c3e68
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clozapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mayne Pharma
- Application
- ANDA203807
- Marketing category
- ANDA
- Marketing start
- 2017-10-26
- Marketing end
- 2022-07-31
- Substance
- CLOZAPINE
- Active strength
- 200 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 |
|---|
| 51862-274-01 | 51862027401 | 100 TABLET in 1 BOTTLE (51862-274-01) | 100 tablet | 2017-10-26 | 0000-00-00 | No | No | Current |
| 51862-274-05 | 51862027405 | 500 TABLET in 1 BOTTLE (51862-274-05) | 500 tablet | 2017-10-26 | 0000-00-00 | No | No | Current |