quetiapine fumarate er

Generic: quetiapine fumarate er

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quetiapine fumarate er
Generic Name quetiapine fumarate er
Labeler direct_rx
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

quetiapine fumarate 150 mg/1

Manufacturer
Direct_rx

Identifiers & Regulatory

Product NDC 72189-586
Product ID 72189-586_23820efc-4df8-9dc9-e063-6394a90a0bb4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209635
Listing Expiration 2026-12-31
Marketing Start 2024-10-02

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189586
Hyphenated Format 72189-586

Supplemental Identifiers

RxCUI
895670
UNII
2S3PL1B6UJ

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name quetiapine fumarate er (source: ndc)
Generic Name quetiapine fumarate er (source: ndc)
Application Number ANDA209635 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-586-30)
source: ndc

Packages (1)

72189-586-30 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-586-30)

Ingredients (1)

quetiapine fumarate (150 mg/1)

Linked Drug Pages (1)

Quetiapine Fumarate ER ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "23820efc-4df8-9dc9-e063-6394a90a0bb4", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["895670"], "spl_set_id": ["23820efc-4df7-9dc9-e063-6394a90a0bb4"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-586-30)", "package_ndc": "72189-586-30", "marketing_start_date": "20241002"}], "brand_name": "Quetiapine Fumarate ER", "product_id": "72189-586_23820efc-4df8-9dc9-e063-6394a90a0bb4", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-586", "generic_name": "Quetiapine Fumarate ER", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate ER", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "150 mg/1"}], "application_number": "ANDA209635", "marketing_category": "ANDA", "marketing_start_date": "20241002", "listing_expiration_date": "20261231"}