trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 100 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7137
Product ID 68788-7137_591e35ff-e385-4ed7-89db-08197a35491e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205253
Listing Expiration 2026-12-31
Marketing Start 2018-04-10

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887137
Hyphenated Format 68788-7137

Supplemental Identifiers

RxCUI
856373
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
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-7137-1)
  • 30 TABLET in 1 BOTTLE (68788-7137-3)
  • 60 TABLET in 1 BOTTLE (68788-7137-6)
  • 28 TABLET in 1 BOTTLE (68788-7137-8)
  • 90 TABLET in 1 BOTTLE (68788-7137-9)
source: ndc

Packages (5)

68788-7137-1 100 TABLET in 1 BOTTLE (68788-7137-1) 68788-7137-3 30 TABLET in 1 BOTTLE (68788-7137-3) 68788-7137-6 60 TABLET in 1 BOTTLE (68788-7137-6) 68788-7137-8 28 TABLET in 1 BOTTLE (68788-7137-8) 68788-7137-9 90 TABLET in 1 BOTTLE (68788-7137-9)

Ingredients (1)

trazodone hydrochloride (100 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": "591e35ff-e385-4ed7-89db-08197a35491e", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856373"], "spl_set_id": ["67d2a90a-3036-409c-aa32-937c55076547"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7137-1)", "package_ndc": "68788-7137-1", "marketing_start_date": "20180410"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7137-3)", "package_ndc": "68788-7137-3", "marketing_start_date": "20180410"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7137-6)", "package_ndc": "68788-7137-6", "marketing_start_date": "20180410"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (68788-7137-8)", "package_ndc": "68788-7137-8", "marketing_start_date": "20180410"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7137-9)", "package_ndc": "68788-7137-9", "marketing_start_date": "20180410"}], "brand_name": "Trazodone Hydrochloride", "product_id": "68788-7137_591e35ff-e385-4ed7-89db-08197a35491e", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "68788-7137", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20180410", "listing_expiration_date": "20261231"}