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 50090-5218
Product ID 50090-5218_b80aed44-291f-4708-8f9e-6ccf9d761a33
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 500905218
Hyphenated Format 50090-5218

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
  • 30 TABLET in 1 BOTTLE (50090-5218-0)
  • 100 TABLET in 1 BOTTLE (50090-5218-1)
  • 60 TABLET in 1 BOTTLE (50090-5218-6)
  • 45 TABLET in 1 BOTTLE (50090-5218-8)
  • 90 TABLET in 1 BOTTLE (50090-5218-9)
source: ndc

Packages (5)

50090-5218-0 30 TABLET in 1 BOTTLE (50090-5218-0) 50090-5218-1 100 TABLET in 1 BOTTLE (50090-5218-1) 50090-5218-6 60 TABLET in 1 BOTTLE (50090-5218-6) 50090-5218-8 45 TABLET in 1 BOTTLE (50090-5218-8) 50090-5218-9 90 TABLET in 1 BOTTLE (50090-5218-9)

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": "b80aed44-291f-4708-8f9e-6ccf9d761a33", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["3df90104-ef2c-4a82-b007-9843c43969ae"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5218-0)", "package_ndc": "50090-5218-0", "marketing_start_date": "20201006"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-5218-1)", "package_ndc": "50090-5218-1", "marketing_start_date": "20201006"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-5218-6)", "package_ndc": "50090-5218-6", "marketing_start_date": "20201006"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (50090-5218-8)", "package_ndc": "50090-5218-8", "marketing_start_date": "20221027"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5218-9)", "package_ndc": "50090-5218-9", "marketing_start_date": "20201006"}], "brand_name": "Trazodone Hydrochloride", "product_id": "50090-5218_b80aed44-291f-4708-8f9e-6ccf9d761a33", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "50090-5218", "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"}