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 Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
J6292F8L3DHALOPERIDOL52-86-8HALOPERIDOL

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Haloperidol - State of Florida DOH Central PharmacyState of Florida DOH Central Pharmacy2013-09-11HUMAN PRESCRIPTION DRUG LABEL1