CHLORPROMAZINE HYDROCHLORIDE
- Product NDC
- 52584-397
- 11-digit product format
- 525840397
- Labeler code
- 52584
- Product ID
- 52584-397_5988b250-29e5-4477-a4c9-a57a4031af8a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORPROMAZINE HYDROCHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA083329
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- Marketing end
- 2024-07-31
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 25 mg/mL
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 52584-397-31 | 52584039731 | 1 AMPULE in 1 BAG (52584-397-31) > 1 mL in 1 AMPULE | 1 ampule | 2018-07-02 | 2024-07-31 | No | No | Current |