Clozapine
- Product NDC
- 72721-1770
- 11-digit product format
- 727211770
- Labeler code
- 72721
- Product ID
- 72721-1770_ffcdd0e6-9db0-4387-8822-781eda375bf8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clozapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Heartwood Pharma
- Application
- NDA019758
- Marketing category
- NDA
- Marketing start
- 2019-07-30
- Marketing end
- 0000-00-00
- Substance
- CLOZAPINE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72721-1770-5 | 72721177005 | 100 TABLET in 1 BOTTLE (72721-1770-5) | 100 tablet | 2019-07-30 | 0000-00-00 | No | No | Current |