risperidone

Product NDC

68071-3369

11-digit product format

680713369

Labeler code

68071

Product ID

68071-3369_553f3a02-abe3-668c-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

risperidone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA078040

Marketing category

ANDA

Marketing start

2008-11-13

Marketing end

0000-00-00

Substance

RISPERIDONE

Active strength

2 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record