Chlorpromazine hydrochloride
- Product NDC
- 68083-534
- 11-digit product format
- 680830534
- Labeler code
- 68083
- Product ID
- 68083-534_ffd998aa-4c6f-4463-b77c-9dc2e722b948
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- Gland Pharma Limited
- Application
- ANDA216911
- Marketing category
- ANDA
- Marketing start
- 2024-10-04
- 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 |
|---|
| 68083-534-25 | 68083053425 | 25 VIAL in 1 CARTON (68083-534-25) / 2 mL in 1 VIAL | 25 vial | 2024-10-04 | No | No | Historical |