trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 50 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8371
Product ID 0615-8371_da411052-e55d-4d7c-960e-c085a6554408
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071523
Listing Expiration 2026-12-31
Marketing Start 2020-10-01

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06158371
Hyphenated Format 0615-8371

Supplemental Identifiers

RxCUI
856364 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 BLISTER PACK (0615-8371-05)
  • 7 TABLET in 1 BLISTER PACK (0615-8371-07)
  • 14 TABLET in 1 BLISTER PACK (0615-8371-14)
  • 28 TABLET in 1 BLISTER PACK (0615-8371-28)
  • 30 TABLET in 1 BLISTER PACK (0615-8371-39)
source: ndc

Packages (5)

0615-8371-05 15 TABLET in 1 BLISTER PACK (0615-8371-05) 0615-8371-07 7 TABLET in 1 BLISTER PACK (0615-8371-07) 0615-8371-14 14 TABLET in 1 BLISTER PACK (0615-8371-14) 0615-8371-28 28 TABLET in 1 BLISTER PACK (0615-8371-28) 0615-8371-39 30 TABLET in 1 BLISTER PACK (0615-8371-39)

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": "da411052-e55d-4d7c-960e-c085a6554408", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856377"], "spl_set_id": ["310c4b81-d2cf-4014-873d-e71d036105de"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BLISTER PACK (0615-8371-05)", "package_ndc": "0615-8371-05", "marketing_start_date": "20220211"}, {"sample": false, "description": "7 TABLET in 1 BLISTER PACK (0615-8371-07)", "package_ndc": "0615-8371-07", "marketing_start_date": "20221208"}, {"sample": false, "description": "14 TABLET in 1 BLISTER PACK (0615-8371-14)", "package_ndc": "0615-8371-14", "marketing_start_date": "20221208"}, {"sample": false, "description": "28 TABLET in 1 BLISTER PACK (0615-8371-28)", "package_ndc": "0615-8371-28", "marketing_start_date": "20240329"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8371-39)", "package_ndc": "0615-8371-39", "marketing_start_date": "20220211"}], "brand_name": "Trazodone Hydrochloride", "product_id": "0615-8371_da411052-e55d-4d7c-960e-c085a6554408", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "0615-8371", "generic_name": "Trazodone Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "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": "20201001", "listing_expiration_date": "20261231"}