Chlorpromazine Hydrochloride
- Product NDC
- 67046-1633
- 11-digit product format
- 670461633
- Labeler code
- 67046
- Product ID
- 67046-1633_472ea988-e54b-93cd-e063-6394a90ada7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA214827
- Marketing category
- ANDA
- Marketing start
- 2025-12-30
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9WP59609J6 | CHLORPROMAZINE HYDROCHLORIDE | 69-09-0 | CHLORPROMAZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 67046-1633-3 | 67046163303 | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (67046-1633-3) | 2025-12-30 | No | No | Historical |