CLOZAPINE
- Product NDC
- 70518-3391
- 11-digit product format
- 705183391
- Labeler code
- 70518
- Product ID
- 70518-3391_da7da9c8-3754-998a-e053-2a95a90a9cf2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CLOZAPINE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206433
- Marketing category
- ANDA
- Marketing start
- 2022-03-17
- Marketing end
- 0000-00-00
- Substance
- CLOZAPINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-3391-0 | 70518339100 | 100 POUCH in 1 BOX (70518-3391-0) > 1 TABLET in 1 POUCH (70518-3391-1) | 100 pouch | 2022-03-17 | 0000-00-00 | No | No | Current |