trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-154
Product ID 72789-154_37669b5c-f93d-34d3-e063-6394a90a677d
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 72789154
Hyphenated Format 72789-154

Supplemental Identifiers

RxCUI
856377
UPC
0372789154909
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
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-154-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-154-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-154-90)
source: ndc

Packages (3)

72789-154-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-154-30) 72789-154-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-154-60) 72789-154-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-154-90)

Ingredients (1)

trazodone hydrochloride (50 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": "37669b5c-f93d-34d3-e063-6394a90a677d", "openfda": {"upc": ["0372789154909"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["04c287ca-5efa-469d-ab39-ff16d9b1e0b3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-154-30)", "package_ndc": "72789-154-30", "marketing_start_date": "20210201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-154-60)", "package_ndc": "72789-154-60", "marketing_start_date": "20210201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-154-90)", "package_ndc": "72789-154-90", "marketing_start_date": "20210112"}], "brand_name": "Trazodone Hydrochloride", "product_id": "72789-154_37669b5c-f93d-34d3-e063-6394a90a677d", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "72789-154", "generic_name": "Trazodone Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}