Haloperidol
- Product NDC
- 70518-0831
- 11-digit product format
- 705180831
- Labeler code
- 70518
- Product ID
- 70518-0831_e26fd2ac-f09d-7836-e053-2995a90a8d5d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077580
- Marketing category
- ANDA
- Marketing start
- 2017-11-09
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-0831-0 | 70518083100 | 30 TABLET in 1 BLISTER PACK (70518-0831-0) | 30 tablet | 2017-11-09 | 0000-00-00 | No | No | Current |
| 70518-0831-1 | 70518083101 | 100 POUCH in 1 BOX (70518-0831-1) > 1 TABLET in 1 POUCH (70518-0831-2) | 100 pouch | 2021-02-26 | 0000-00-00 | No | No | Current |