Haldol
- Product NDC
- 50458-255
- 11-digit product format
- 504580255
- Labeler code
- 50458
- Product ID
- 50458-255_f43303ba-8106-11eb-ac20-3addfb2ca371
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- Janssen Pharmaceuticals, Inc.
- Application
- NDA015923
- Marketing category
- NDA
- Marketing start
- 1971-05-18
- Marketing end
- 2050-08-02
- Substance
- HALOPERIDOL LACTATE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- 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 |
|---|
| 50458-255-01 | 50458025501 | 10 AMPULE in 1 BOX (50458-255-01) > 1 mL in 1 AMPULE | 10 ampule | 1971-05-18 | 0000-00-00 | No | No | Current |