quetiapine

Generic: quetiapine

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quetiapine
Generic Name quetiapine
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

quetiapine fumarate 200 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-401
Product ID 71205-401_fbe8f179-fe43-43a4-b592-a31f2ec6aede
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202152
Listing Expiration 2026-12-31
Marketing Start 2012-03-28

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205401
Hyphenated Format 71205-401

Supplemental Identifiers

RxCUI
317174
UPC
0371205401306
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 (71205-401-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-401-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-401-90)
source: ndc

Packages (3)

71205-401-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-401-30) 71205-401-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-401-60) 71205-401-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-401-90)

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": "fbe8f179-fe43-43a4-b592-a31f2ec6aede", "openfda": {"upc": ["0371205401306"], "unii": ["2S3PL1B6UJ"], "rxcui": ["317174"], "spl_set_id": ["7a090720-fd90-4976-9aa2-41812106eb70"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-401-30)", "package_ndc": "71205-401-30", "marketing_start_date": "20200213"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-401-60)", "package_ndc": "71205-401-60", "marketing_start_date": "20200213"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-401-90)", "package_ndc": "71205-401-90", "marketing_start_date": "20200213"}], "brand_name": "Quetiapine", "product_id": "71205-401_fbe8f179-fe43-43a4-b592-a31f2ec6aede", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71205-401", "generic_name": "Quetiapine", "labeler_name": "Proficient Rx LP", "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": "20120328", "listing_expiration_date": "20261231"}