trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6603
Product ID 50090-6603_30db7ddc-f345-457d-a04f-1258502e147e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205253
Listing Expiration 2026-12-31
Marketing Start 2017-12-11

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906603
Hyphenated Format 50090-6603

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 ANDA205253 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-6603-0)
source: ndc

Packages (1)

Ingredients (1)

trazodone hydrochloride (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30db7ddc-f345-457d-a04f-1258502e147e", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["007f38e0-653b-43e4-a1c1-b59997b2762a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6603-0)", "package_ndc": "50090-6603-0", "marketing_start_date": "20230822"}], "brand_name": "Trazodone Hydrochloride", "product_id": "50090-6603_30db7ddc-f345-457d-a04f-1258502e147e", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "50090-6603", "generic_name": "Trazodone Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}