Haloperidol Decanoate

Product NDC

0703-7011

11-digit product format

007037011

Labeler code

0703

Product ID

0703-7011_0ca22830-67fa-49ec-842b-e1846c0e162c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Haloperidol Decanoate

Dosage form

INJECTION

Route

INTRAMUSCULAR

Labeler

Teva Parenteral Medicines, Inc.

Application

ANDA075393

Marketing category

ANDA

Marketing start

1999-06-04

Marketing end

2020-12-31

Substance

HALOPERIDOL DECANOATE

Active strength

50 mg/mL

Pharmacologic classes

Typical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record