Loperamide Hydrochloride

Product NDC

50436-3974

11-digit product format

504363974

Labeler code

50436

Product ID

50436-3974_ab0b3856-ca6c-4e62-9c16-63c04b8e1bd8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

loperamide hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA072741

Marketing category

ANDA

Marketing start

1991-09-18

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