Haloperidol
- Product NDC
- 70518-1529
- 11-digit product format
- 705181529
- Labeler code
- 70518
- Product ID
- 70518-1529_93fd9282-5fe0-0b5b-e053-2a95a90a2db2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071209
- Marketing category
- ANDA
- Marketing start
- 2018-10-15
- 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