trazodone hydrochloride
Generic: trazodone hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
trazodone hydrochloride
Generic Name
trazodone hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
trazodone hydrochloride 150 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-4825
Product ID
50090-4825_35fe01ac-7982-454c-b9c8-cf5c3a321c29
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205253
Listing Expiration
2027-12-31
Marketing Start
2017-12-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500904825
Hyphenated Format
50090-4825
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 150 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (50090-4825-2)
- 90 TABLET in 1 BOTTLE (50090-4825-4)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35fe01ac-7982-454c-b9c8-cf5c3a321c29", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["4fcd25d5-e34f-4eea-aeff-aa442651e681"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-4825-2)", "package_ndc": "50090-4825-2", "marketing_start_date": "20200103"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4825-4)", "package_ndc": "50090-4825-4", "marketing_start_date": "20200103"}], "brand_name": "Trazodone Hydrochloride", "product_id": "50090-4825_35fe01ac-7982-454c-b9c8-cf5c3a321c29", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "50090-4825", "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": "150 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20271231"}