Haloperidol
- Product NDC
- 53808-0840
- 11-digit product format
- 538080840
- Labeler code
- 53808
- Product ID
- 53808-0840_b252f4a8-1e2d-48b0-9296-dc9681acdcf7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA070278
- Marketing category
- ANDA
- Marketing start
- 2013-01-01
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| J6292F8L3D | HALOPERIDOL | 52-86-8 | HALOPERIDOL |