Chlorpromazine Hydrochloride
- Product NDC
- 24338-403
- 11-digit product format
- 243380403
- Labeler code
- 24338
- Product ID
- 24338-403_d3c3c2cc-ad9e-436a-a044-555b3544c202
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- CONCENTRATE
- Route
- ORAL
- Labeler
- Azurity Pharmaceuticals, Inc.
- Application
- ANDA214542
- Marketing category
- ANDA
- Marketing start
- 2021-08-02
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 30 mg/mL
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 24338-403-12 | 24338040312 | 120 mL in 1 BOTTLE, PLASTIC (24338-403-12) | 120 ml | 2021-08-02 | 0000-00-00 | No | No | Current |