Loperamide Hydrochloride

Product NDC

68788-9079

11-digit product format

687889079

Labeler code

68788

Product ID

68788-9079_33aaec1c-3942-4d3b-83f8-2e57991304aa

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Loperamide Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA073192

Marketing category

ANDA

Marketing start

2011-01-28

Marketing end

0000-00-00

Substance

LOPERAMIDE HYDROCHLORIDE

Active strength

2 mg/1

Pharmacologic classes

Opioid Agonist [EPC],Opioid Agonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record