Haloperidol
- Product NDC
- 63187-842
- 11-digit product format
- 631870842
- Labeler code
- 63187
- Product ID
- 63187-842_2274db0b-42a3-484e-941c-990bad99df65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA071209
- Marketing category
- ANDA
- Marketing start
- 1986-11-17
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-842 | HALOPERIDOL TABLET [PROFICIENT RX LP] | 3 | Legacy NDC | 20191113_e5c28155-a7a5-4d1e-aae5-99408b5f457c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-842-03 | 63187084203 | 3 TABLET in 1 BOTTLE (63187-842-03) | 3 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 63187-842-30 | 63187084230 | 30 TABLET in 1 BOTTLE (63187-842-30) | 30 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 63187-842-60 | 63187084260 | 60 TABLET in 1 BOTTLE (63187-842-60) | 60 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 63187-842-90 | 63187084290 | 90 TABLET in 1 BOTTLE (63187-842-90) | 90 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |