trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 150 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-815
Product ID 71205-815_3c8c3d2b-9108-40fa-90d9-6ed545cf6549
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202180
Listing Expiration 2026-12-31
Marketing Start 2013-11-27

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205815
Hyphenated Format 71205-815

Supplemental Identifiers

RxCUI
856364
UPC
0371205815301
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 ANDA202180 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-815-30)
  • 60 TABLET in 1 BOTTLE (71205-815-60)
  • 90 TABLET in 1 BOTTLE (71205-815-90)
source: ndc

Packages (3)

71205-815-30 30 TABLET in 1 BOTTLE (71205-815-30) 71205-815-60 60 TABLET in 1 BOTTLE (71205-815-60) 71205-815-90 90 TABLET in 1 BOTTLE (71205-815-90)

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": "3c8c3d2b-9108-40fa-90d9-6ed545cf6549", "openfda": {"upc": ["0371205815301"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["3c8c3d2b-9108-40fa-90d9-6ed545cf6549"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-815-30)", "package_ndc": "71205-815-30", "marketing_start_date": "20230619"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-815-60)", "package_ndc": "71205-815-60", "marketing_start_date": "20230619"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-815-90)", "package_ndc": "71205-815-90", "marketing_start_date": "20230619"}], "brand_name": "Trazodone Hydrochloride", "product_id": "71205-815_3c8c3d2b-9108-40fa-90d9-6ed545cf6549", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "71205-815", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA202180", "marketing_category": "ANDA", "marketing_start_date": "20131127", "listing_expiration_date": "20261231"}