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 150 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-079
Product ID 72789-079_4019c854-3393-5b53-e063-6394a90abd16
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071525
Listing Expiration 2026-12-31
Marketing Start 2020-03-11

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789079
Hyphenated Format 72789-079

Supplemental Identifiers

RxCUI
856364
UPC
0372789079301
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 ANDA071525 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-079-30)
source: ndc

Packages (1)

72789-079-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-079-30)

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": "4019c854-3393-5b53-e063-6394a90abd16", "openfda": {"upc": ["0372789079301"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["9b022ae9-dd52-43ae-804b-ddf8e7cfd530"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-079-30)", "package_ndc": "72789-079-30", "marketing_start_date": "20200406"}], "brand_name": "Trazodone Hydrochloride", "product_id": "72789-079_4019c854-3393-5b53-e063-6394a90abd16", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "72789-079", "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": "150 mg/1"}], "application_number": "ANDA071525", "marketing_category": "ANDA", "marketing_start_date": "20200311", "listing_expiration_date": "20261231"}