trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

trazodone hydrochloride 50 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4410
Product ID 68071-4410_1a8bc751-c265-821d-e063-6394a90a49c2
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 680714410
Hyphenated Format 68071-4410

Supplemental Identifiers

RxCUI
856377
UPC
0368071441093
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
  • 20 TABLET in 1 BOTTLE (68071-4410-2)
  • 30 TABLET in 1 BOTTLE (68071-4410-3)
  • 45 TABLET in 1 BOTTLE (68071-4410-4)
  • 56 TABLET in 1 BOTTLE (68071-4410-5)
  • 60 TABLET in 1 BOTTLE (68071-4410-6)
  • 28 TABLET in 1 BOTTLE (68071-4410-8)
  • 90 TABLET in 1 BOTTLE (68071-4410-9)
source: ndc

Packages (7)

Ingredients (1)

trazodone hydrochloride (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a8bc751-c265-821d-e063-6394a90a49c2", "openfda": {"upc": ["0368071441093"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["6adb446d-cd2f-3d6b-e053-2991aa0a2114"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-4410-2)", "package_ndc": "68071-4410-2", "marketing_start_date": "20180427"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4410-3)", "package_ndc": "68071-4410-3", "marketing_start_date": "20180427"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (68071-4410-4)", "package_ndc": "68071-4410-4", "marketing_start_date": "20180427"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (68071-4410-5)", "package_ndc": "68071-4410-5", "marketing_start_date": "20180427"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-4410-6)", "package_ndc": "68071-4410-6", "marketing_start_date": "20180427"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (68071-4410-8)", "package_ndc": "68071-4410-8", "marketing_start_date": "20180427"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-4410-9)", "package_ndc": "68071-4410-9", "marketing_start_date": "20180427"}], "brand_name": "Trazodone Hydrochloride", "product_id": "68071-4410_1a8bc751-c265-821d-e063-6394a90a49c2", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "68071-4410", "generic_name": "Trazodone Hydrochloride", "labeler_name": "NuCare 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"}