Loperamide Hydrochloride

Product NDC

68071-4075

11-digit product format

680714075

Labeler code

68071

Product ID

68071-4075_5812a533-90fa-6e6d-e053-2a91aa0afc0c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Loperamide Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCare pharmceuticals,Inc.

Application

ANDA073192

Marketing category

ANDA

Marketing start

1993-05-01

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