Haloperidol

Product NDC

0093-9604

11-digit product format

000939604

Labeler code

0093

Product ID

0093-9604_d11b56e9-123c-4c7b-bf1d-26e07901c370

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Haloperidol lactate

Dosage form

SOLUTION, CONCENTRATE

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA071617

Marketing category

ANDA

Marketing start

1988-12-01

Marketing end

2020-05-31

Substance

HALOPERIDOL LACTATE

Active strength

2 mg/mL

Pharmacologic classes

Typical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record