trazodone hydrochloride
Generic: trazodone hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
trazodone hydrochloride
Generic Name
trazodone hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
trazodone hydrochloride 150 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-3024
Product ID
71335-3024_a54aaa58-01e7-492c-ab4b-3eae98e4b87f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204852
Listing Expiration
2026-12-31
Marketing Start
2015-09-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713353024
Hyphenated Format
71335-3024
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
ANDA204852 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 150 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (71335-3024-1)
- 1000 TABLET in 1 BOTTLE (71335-3024-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a54aaa58-01e7-492c-ab4b-3eae98e4b87f", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["24b5eee4-4210-4b90-a695-11e6a5868988"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-3024-1)", "package_ndc": "71335-3024-1", "marketing_start_date": "20251204"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-3024-2)", "package_ndc": "71335-3024-2", "marketing_start_date": "20251204"}], "brand_name": "TRAZODONE HYDROCHLORIDE", "product_id": "71335-3024_a54aaa58-01e7-492c-ab4b-3eae98e4b87f", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "71335-3024", "generic_name": "TRAZODONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAZODONE HYDROCHLORIDE", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA204852", "marketing_category": "ANDA", "marketing_start_date": "20150915", "listing_expiration_date": "20261231"}