Haloperidol

Product NDC

51991-933

11-digit product format

519910933

Labeler code

51991

Product ID

51991-933_09846faf-2392-4faa-8c80-9f3176d92052

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Haloperidol Lactate

Dosage form

INJECTION

Route

INTRAMUSCULAR

Labeler

Breckenridge Pharmaceutical, Inc.

Application

ANDA076774

Marketing category

ANDA

Marketing start

2016-01-04

Marketing end

2019-11-30

Substance

HALOPERIDOL LACTATE

Active strength

5 mg/mL

Pharmacologic classes

Typical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record