Chlorpromazine Hydrochloride
- Product NDC
- 64950-240
- 11-digit product format
- 649500240
- Labeler code
- 64950
- Product ID
- 64950-240_1a5bb73f-a88d-4f24-985d-eb7bd0917461
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORPROMAZINE HYDROCHLORIDE
- Dosage form
- CONCENTRATE
- Route
- ORAL
- Labeler
- Genus Lifesciences Inc.
- Application
- ANDA214542
- Marketing category
- ANDA
- Marketing start
- 2021-08-10
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 30 mg/mL
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 64950-240-12 | 64950024012 | 120 mL in 1 BOTTLE, PLASTIC (64950-240-12) | 120 ml | 2021-08-10 | 0000-00-00 | No | No | Current |