Haloperidol

Product NDC

0781-1398

11-digit product format

007811398

Labeler code

0781

Product ID

0781-1398_efbe4986-95cd-4ddb-8120-c6feacd2017f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Haloperidol

Dosage form

TABLET

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA071211

Marketing category

ANDA

Marketing start

1988-03-11

Marketing end

2020-12-31

Substance

HALOPERIDOL

Active strength

20 mg/1

Pharmacologic classes

Typical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record