trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 100 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2531
Product ID 72162-2531_6e436507-7029-4e44-9bfd-b4e36573a801
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204852
Listing Expiration 2026-12-31
Marketing Start 2015-09-15

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622531
Hyphenated Format 72162-2531

Supplemental Identifiers

RxCUI
856373
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
  • 100 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72162-2531-0)
  • 100 TABLET in 1 BOTTLE (72162-2531-1)
  • 30 TABLET in 1 BOTTLE (72162-2531-3)
  • 500 TABLET in 1 BOTTLE (72162-2531-5)
  • 90 TABLET in 1 BOTTLE (72162-2531-9)
source: ndc

Packages (5)

72162-2531-0 1000 TABLET in 1 BOTTLE (72162-2531-0) 72162-2531-1 100 TABLET in 1 BOTTLE (72162-2531-1) 72162-2531-3 30 TABLET in 1 BOTTLE (72162-2531-3) 72162-2531-5 500 TABLET in 1 BOTTLE (72162-2531-5) 72162-2531-9 90 TABLET in 1 BOTTLE (72162-2531-9)

Ingredients (1)

trazodone hydrochloride (100 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": "6e436507-7029-4e44-9bfd-b4e36573a801", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856373"], "spl_set_id": ["4370fe5c-1c40-499b-abb5-bca0a39834c6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2531-0)", "package_ndc": "72162-2531-0", "marketing_start_date": "20250919"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2531-1)", "package_ndc": "72162-2531-1", "marketing_start_date": "20250919"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2531-3)", "package_ndc": "72162-2531-3", "marketing_start_date": "20250919"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2531-5)", "package_ndc": "72162-2531-5", "marketing_start_date": "20250919"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-2531-9)", "package_ndc": "72162-2531-9", "marketing_start_date": "20250919"}], "brand_name": "TRAZODONE HYDROCHLORIDE", "product_id": "72162-2531_6e436507-7029-4e44-9bfd-b4e36573a801", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "72162-2531", "generic_name": "TRAZODONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAZODONE HYDROCHLORIDE", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA204852", "marketing_category": "ANDA", "marketing_start_date": "20150915", "listing_expiration_date": "20261231"}