trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 50 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-525
Product ID 71610-525_3ab5bd42-a909-30d0-e063-6394a90aee04
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071523
Listing Expiration 2026-12-31
Marketing Start 2020-11-06

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610525
Hyphenated Format 71610-525

Supplemental Identifiers

RxCUI
856373 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 ANDA071523 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (71610-525-15)
  • 30 TABLET in 1 BOTTLE (71610-525-30)
  • 45 TABLET in 1 BOTTLE (71610-525-45)
  • 60 TABLET in 1 BOTTLE (71610-525-53)
  • 90 TABLET in 1 BOTTLE (71610-525-60)
  • 120 TABLET in 1 BOTTLE (71610-525-70)
source: ndc

Packages (6)

71610-525-15 15 TABLET in 1 BOTTLE (71610-525-15) 71610-525-30 30 TABLET in 1 BOTTLE (71610-525-30) 71610-525-45 45 TABLET in 1 BOTTLE (71610-525-45) 71610-525-53 60 TABLET in 1 BOTTLE (71610-525-53) 71610-525-60 90 TABLET in 1 BOTTLE (71610-525-60) 71610-525-70 120 TABLET in 1 BOTTLE (71610-525-70)

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": "3ab5bd42-a909-30d0-e063-6394a90aee04", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856373", "856377"], "spl_set_id": ["5ab590d8-225f-43f4-bb68-1f2c86f9a886"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (71610-525-15)", "package_ndc": "71610-525-15", "marketing_start_date": "20210208"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71610-525-30)", "package_ndc": "71610-525-30", "marketing_start_date": "20210208"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71610-525-45)", "package_ndc": "71610-525-45", "marketing_start_date": "20210208"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-525-53)", "package_ndc": "71610-525-53", "marketing_start_date": "20210208"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-525-60)", "package_ndc": "71610-525-60", "marketing_start_date": "20210407"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71610-525-70)", "package_ndc": "71610-525-70", "marketing_start_date": "20210208"}], "brand_name": "Trazodone Hydrochloride", "product_id": "71610-525_3ab5bd42-a909-30d0-e063-6394a90aee04", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "71610-525", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA071523", "marketing_category": "ANDA", "marketing_start_date": "20201106", "listing_expiration_date": "20261231"}