trazodone hydrochloride
Generic: trazodone hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
trazodone hydrochloride
Generic Name
trazodone hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
trazodone hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-168
Product ID
72789-168_3766e8ce-b3d7-c8de-e063-6294a90a05d1
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
72789168
Hyphenated Format
72789-168
Supplemental Identifiers
RxCUI
UPC
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
- 100 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-168-30)
- 90 TABLET in 1 BOTTLE, PLASTIC (72789-168-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3766e8ce-b3d7-c8de-e063-6294a90a05d1", "openfda": {"upc": ["0372789168906"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856373"], "spl_set_id": ["614f2c6e-0bb7-43e0-85d8-5eef8eeae208"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-168-30)", "package_ndc": "72789-168-30", "marketing_start_date": "20210325"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-168-90)", "package_ndc": "72789-168-90", "marketing_start_date": "20210222"}], "brand_name": "Trazodone Hydrochloride", "product_id": "72789-168_3766e8ce-b3d7-c8de-e063-6294a90a05d1", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "72789-168", "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": "100 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}