Haloperidol
- Product NDC
- 70518-2893
- 11-digit product format
- 705182893
- Labeler code
- 70518
- Product ID
- 70518-2893_d78697cb-28eb-2d7f-e053-2a95a90a8a58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211061
- Marketing category
- ANDA
- Marketing start
- 2020-09-20
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2893 | HALOPERIDOL TABLET [REMEDYREPACK INC.] | 6 | Legacy NDC | 20250406_64a37c73-a5f0-4e93-b269-ed12f0d77175.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2893-0 | 70518289300 | 30 TABLET in 1 BLISTER PACK (70518-2893-0) | 30 tablet | 2020-09-20 | 0000-00-00 | No | No | Current |