trazodone hydrochloride
Generic: trazodone hydrochloride
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
trazodone hydrochloride
Generic Name
trazodone hydrochloride
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
trazodone hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-366
Product ID
51655-366_49daf198-ebf2-ddd1-e063-6394a90a54d7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071523
Listing Expiration
2027-12-31
Marketing Start
2022-11-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655366
Hyphenated Format
51655-366
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
ANDA071523 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (51655-366-26)
- 30 TABLET in 1 BOTTLE, PLASTIC (51655-366-52)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49daf198-ebf2-ddd1-e063-6394a90a54d7", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["f2f2290f-b53c-3b38-e053-2995a90a157d"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-366-26)", "package_ndc": "51655-366-26", "marketing_start_date": "20230105"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-366-52)", "package_ndc": "51655-366-52", "marketing_start_date": "20221130"}], "brand_name": "Trazodone Hydrochloride", "product_id": "51655-366_49daf198-ebf2-ddd1-e063-6394a90a54d7", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "51655-366", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA071523", "marketing_category": "ANDA", "marketing_start_date": "20221130", "listing_expiration_date": "20271231"}