Chlorpromazine Hydrochloride
- Product NDC
- 70710-1850
- 11-digit product format
- 707101850
- Labeler code
- 70710
- Product ID
- 70710-1850_97106093-2f0a-4cc9-b580-942b015c6c5b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA217275
- Marketing category
- ANDA
- Marketing start
- 2024-03-29
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 25 mg/mL
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70710-1850-7 | 70710185007 | 25 VIAL in 1 CARTON (70710-1850-7) / 2 mL in 1 VIAL (70710-1850-1) | 25 vial | 2024-03-29 | No | No | Historical |