trazodone hydrochloride
Generic: trazodone hydrochloride
Labeler: medsource pharmaceuticalsDrug Facts
Product Profile
Brand Name
trazodone hydrochloride
Generic Name
trazodone hydrochloride
Labeler
medsource pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
trazodone hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
45865-167
Product ID
45865-167_12f16727-8822-5b6c-e063-6394a90a02a6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205253
Listing Expiration
2026-12-31
Marketing Start
2017-12-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
45865167
Hyphenated Format
45865-167
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
- 50 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (45865-167-30)
- 60 TABLET in 1 BOTTLE (45865-167-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "12f16727-8822-5b6c-e063-6394a90a02a6", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["12f1737b-c021-d0f2-e063-6294a90a6f29"], "manufacturer_name": ["Medsource Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (45865-167-30)", "package_ndc": "45865-167-30", "marketing_start_date": "20210908"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (45865-167-60)", "package_ndc": "45865-167-60", "marketing_start_date": "20210408"}], "brand_name": "Trazodone Hydrochloride", "product_id": "45865-167_12f16727-8822-5b6c-e063-6394a90a02a6", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "45865-167", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Medsource Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}