trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler asclemed usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 150 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-675
Product ID 76420-675_1244caf6-4ab7-dd22-e063-6294a90a81bd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205253
Listing Expiration 2026-12-31
Marketing Start 2017-12-11

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420675
Hyphenated Format 76420-675

Supplemental Identifiers

RxCUI
856364 856369 856373 856377
UNII
6E8ZO8LRNM

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (76420-675-01)
  • 30 TABLET in 1 BOTTLE (76420-675-30)
  • 60 TABLET in 1 BOTTLE (76420-675-60)
  • 90 TABLET in 1 BOTTLE (76420-675-90)
source: ndc

Packages (4)

76420-675-01 100 TABLET in 1 BOTTLE (76420-675-01) 76420-675-30 30 TABLET in 1 BOTTLE (76420-675-30) 76420-675-60 60 TABLET in 1 BOTTLE (76420-675-60) 76420-675-90 90 TABLET in 1 BOTTLE (76420-675-90)

Ingredients (1)

trazodone hydrochloride (150 mg/1)

Linked Drug Pages (1)

Trazodone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1244caf6-4ab7-dd22-e063-6294a90a81bd", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856369", "856373", "856377"], "spl_set_id": ["04a676ee-358e-484d-9de4-a9a88d908ba8"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-675-01)", "package_ndc": "76420-675-01", "marketing_start_date": "20240226"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-675-30)", "package_ndc": "76420-675-30", "marketing_start_date": "20240226"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-675-60)", "package_ndc": "76420-675-60", "marketing_start_date": "20240226"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-675-90)", "package_ndc": "76420-675-90", "marketing_start_date": "20240226"}], "brand_name": "Trazodone Hydrochloride", "product_id": "76420-675_1244caf6-4ab7-dd22-e063-6294a90a81bd", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "76420-675", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}