trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 150 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0742
Product ID 71335-0742_337bd3ea-ccd3-7ae8-e063-6394a90a9b8f
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 713350742
Hyphenated Format 71335-0742

Supplemental Identifiers

RxCUI
856364
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
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0742-1)
  • 60 TABLET in 1 BOTTLE (71335-0742-2)
  • 90 TABLET in 1 BOTTLE (71335-0742-3)
  • 18 TABLET in 1 BOTTLE (71335-0742-4)
  • 100 TABLET in 1 BOTTLE (71335-0742-5)
  • 45 TABLET in 1 BOTTLE (71335-0742-6)
  • 180 TABLET in 1 BOTTLE (71335-0742-7)
source: ndc

Packages (7)

71335-0742-1 30 TABLET in 1 BOTTLE (71335-0742-1) 71335-0742-2 60 TABLET in 1 BOTTLE (71335-0742-2) 71335-0742-3 90 TABLET in 1 BOTTLE (71335-0742-3) 71335-0742-4 18 TABLET in 1 BOTTLE (71335-0742-4) 71335-0742-5 100 TABLET in 1 BOTTLE (71335-0742-5) 71335-0742-6 45 TABLET in 1 BOTTLE (71335-0742-6) 71335-0742-7 180 TABLET in 1 BOTTLE (71335-0742-7)

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": "337bd3ea-ccd3-7ae8-e063-6394a90a9b8f", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["65ef34fb-8fe4-4e9d-9068-98702515ffeb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0742-1)", "package_ndc": "71335-0742-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0742-2)", "package_ndc": "71335-0742-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0742-3)", "package_ndc": "71335-0742-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-0742-4)", "package_ndc": "71335-0742-4", "marketing_start_date": "20220209"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0742-5)", "package_ndc": "71335-0742-5", "marketing_start_date": "20220209"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-0742-6)", "package_ndc": "71335-0742-6", "marketing_start_date": "20220209"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0742-7)", "package_ndc": "71335-0742-7", "marketing_start_date": "20220209"}], "brand_name": "Trazodone Hydrochloride", "product_id": "71335-0742_337bd3ea-ccd3-7ae8-e063-6394a90a9b8f", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "71335-0742", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}