Haloperidol

Product NDC

70518-0023

11-digit product format

705180023

Labeler code

70518

Product ID

70518-0023_9e70b833-ad99-3346-e053-2a95a90aa122

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

haloperidol

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA070278

Marketing category

ANDA

Marketing start

2017-11-30

Marketing end

0000-00-00

Substance

HALOPERIDOL

Active strength

10 mg/1

Pharmacologic classes

Typical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record