trazodone hcl

Generic: trazodone hcl

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hcl
Generic Name trazodone hcl
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 300 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-569
Product ID 72189-569_1fd0fc6d-5b1d-9f6a-e063-6394a90a3b7c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202180
Listing Expiration 2026-12-31
Marketing Start 2024-08-16

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189569
Hyphenated Format 72189-569

Supplemental Identifiers

RxCUI
856369
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 hcl (source: ndc)
Generic Name trazodone hcl (source: ndc)
Application Number ANDA202180 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-569-30)
source: ndc

Packages (1)

72189-569-30 30 TABLET in 1 BOTTLE (72189-569-30)

Ingredients (1)

trazodone hydrochloride (300 mg/1)

Linked Drug Pages (1)

Trazodone HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1fd0fc6d-5b1d-9f6a-e063-6394a90a3b7c", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856369"], "spl_set_id": ["1fd0fc6d-5b1c-9f6a-e063-6394a90a3b7c"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-569-30)", "package_ndc": "72189-569-30", "marketing_start_date": "20240816"}], "brand_name": "Trazodone HCL", "product_id": "72189-569_1fd0fc6d-5b1d-9f6a-e063-6394a90a3b7c", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "72189-569", "generic_name": "Trazodone HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone HCL", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA202180", "marketing_category": "ANDA", "marketing_start_date": "20240816", "listing_expiration_date": "20261231"}