quetiapine

Generic: quetiapine

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quetiapine
Generic Name quetiapine
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

quetiapine fumarate 200 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4927
Product ID 50090-4927_7286b27f-eb5f-4f5f-ab30-a8604f1d59f4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202152
Listing Expiration 2026-12-31
Marketing Start 2015-12-01

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904927
Hyphenated Format 50090-4927

Supplemental Identifiers

RxCUI
317174
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 (source: ndc)
Generic Name quetiapine (source: ndc)
Application Number ANDA202152 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-4927-0)
source: ndc

Packages (1)

50090-4927-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-4927-0)

Ingredients (1)

quetiapine fumarate (200 mg/1)

Linked Drug Pages (1)

Quetiapine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7286b27f-eb5f-4f5f-ab30-a8604f1d59f4", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["317174"], "spl_set_id": ["2dffb8fa-15be-496b-9fa7-658d5acd7c17"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4927-0)", "package_ndc": "50090-4927-0", "marketing_start_date": "20200220"}], "brand_name": "Quetiapine", "product_id": "50090-4927_7286b27f-eb5f-4f5f-ab30-a8604f1d59f4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-4927", "generic_name": "Quetiapine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "200 mg/1"}], "application_number": "ANDA202152", "marketing_category": "ANDA", "marketing_start_date": "20151201", "listing_expiration_date": "20261231"}