trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: advanced rx of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler advanced rx of tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 50 mg/1

Manufacturer
Advanced Rx of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0502
Product ID 80425-0502_30ca7888-edc4-b659-e063-6294a90ab232
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204852
Listing Expiration 2026-12-31
Marketing Start 2025-03-20

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250502
Hyphenated Format 80425-0502

Supplemental Identifiers

RxCUI
856377
UNII
6E8ZO8LRNM

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 trazodone hydrochloride (source: ndc)
Generic Name trazodone hydrochloride (source: ndc)
Application Number ANDA204852 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (80425-0502-1)
  • 60 TABLET in 1 BOTTLE (80425-0502-2)
  • 90 TABLET in 1 BOTTLE (80425-0502-3)
source: ndc

Packages (3)

80425-0502-1 30 TABLET in 1 BOTTLE (80425-0502-1) 80425-0502-2 60 TABLET in 1 BOTTLE (80425-0502-2) 80425-0502-3 90 TABLET in 1 BOTTLE (80425-0502-3)

Ingredients (1)

trazodone hydrochloride (50 mg/1)

Linked Drug Pages (1)

TRAZODONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "30ca7888-edc4-b659-e063-6294a90ab232", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["30ca6faa-316d-5754-e063-6394a90a7eff"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0502-1)", "package_ndc": "80425-0502-1", "marketing_start_date": "20250320"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0502-2)", "package_ndc": "80425-0502-2", "marketing_start_date": "20250320"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0502-3)", "package_ndc": "80425-0502-3", "marketing_start_date": "20250320"}], "brand_name": "TRAZODONE HYDROCHLORIDE", "product_id": "80425-0502_30ca7888-edc4-b659-e063-6294a90ab232", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "80425-0502", "generic_name": "TRAZODONE HYDROCHLORIDE", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAZODONE HYDROCHLORIDE", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA204852", "marketing_category": "ANDA", "marketing_start_date": "20250320", "listing_expiration_date": "20261231"}