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
50090-7439
Product ID
50090-7439_81b9e7a1-dd24-41c0-95f5-5fe43546c412
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202180
Listing Expiration
2026-12-31
Marketing Start
2013-11-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907439
Hyphenated Format
50090-7439
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
ANDA202180 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 150 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (50090-7439-2)
- 90 TABLET in 1 BOTTLE (50090-7439-4)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "81b9e7a1-dd24-41c0-95f5-5fe43546c412", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["be0dc037-d30a-4f07-ab7c-1695637b3740"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7439-2)", "package_ndc": "50090-7439-2", "marketing_start_date": "20241106"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7439-4)", "package_ndc": "50090-7439-4", "marketing_start_date": "20241106"}], "brand_name": "Trazodone Hydrochloride", "product_id": "50090-7439_81b9e7a1-dd24-41c0-95f5-5fe43546c412", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "50090-7439", "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": "ANDA202180", "marketing_category": "ANDA", "marketing_start_date": "20131127", "listing_expiration_date": "20261231"}