Quetiapine

Product NDC

70518-1823

11-digit product format

705181823

Labeler code

70518

Product ID

70518-1823_840333e5-0693-3d23-e053-2a91aa0a79f5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Quetiapine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA209635

Marketing category

ANDA

Marketing start

2019-01-24

Marketing end

0000-00-00

Substance

QUETIAPINE FUMARATE

Active strength

300 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record