trazodone hydrochloride
Generic: trazodone hydrochloride
Labeler: avkareDrug Facts
Product Profile
Brand Name
trazodone hydrochloride
Generic Name
trazodone hydrochloride
Labeler
avkare
Dosage Form
TABLET
Routes
Active Ingredients
trazodone hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42291-868
Product ID
42291-868_4cc4b32a-0db0-e922-e063-6294a90ab8cd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071523
Listing Expiration
2027-12-31
Marketing Start
2020-11-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42291868
Hyphenated Format
42291-868
Supplemental Identifiers
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
- 1000 TABLET in 1 BOTTLE (42291-868-10)
- 90 TABLET in 1 BOTTLE (42291-868-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4cc4b32a-0db0-e922-e063-6294a90ab8cd", "openfda": {"unii": ["6E8ZO8LRNM"], "spl_set_id": ["b3723265-7455-c25c-e053-2a95a90a379b"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (42291-868-10)", "package_ndc": "42291-868-10", "marketing_start_date": "20201106"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-868-90)", "package_ndc": "42291-868-90", "marketing_start_date": "20201106"}], "brand_name": "Trazodone Hydrochloride", "product_id": "42291-868_4cc4b32a-0db0-e922-e063-6294a90ab8cd", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "42291-868", "generic_name": "Trazodone Hydrochloride", "labeler_name": "AvKARE", "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": "20201106", "listing_expiration_date": "20271231"}