Haloperidol Decanoate
- Product NDC
- 0703-7021
- 11-digit product format
- 007037021
- Labeler code
- 0703
- Product ID
- 0703-7021_0ca22830-67fa-49ec-842b-e1846c0e162c
- 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
- 2021-07-31
- Substance
- HALOPERIDOL DECANOATE
- Active strength
- 100 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0703-7021-03 | 00703702103 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-7021-03) > 1 mL in 1 VIAL, SINGLE-DOSE (0703-7021-01) | 1999-06-04 | 2021-07-31 | No | No | Current |