Haloperidol Decanoate
- Product NDC
- 0703-7121
- 11-digit product format
- 007037121
- Labeler code
- 0703
- Product ID
- 0703-7121_b2959320-817c-4033-9765-1e87cab5b910
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol Decanoate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- Teva Parenteral Medicines, Inc.
- Application
- ANDA075393
- Marketing category
- ANDA
- Marketing start
- 1999-06-04
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL DECANOATE
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0703-7121-03 | 00703712103 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-7121-03) > 1 mL in 1 VIAL, SINGLE-DOSE (0703-7121-01) | 1999-06-04 | 0000-00-00 | No | No | Current |