trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: aurolife pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler aurolife pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 50 mg/1

Manufacturer
Aurolife Pharma LLC

Identifiers & Regulatory

Product NDC 13107-079
Product ID 13107-079_db4e6aff-149f-4f16-9512-e81e0c3e6900
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204852
Listing Expiration 2026-12-31
Marketing Start 2015-09-15

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 13107079
Hyphenated Format 13107-079

Supplemental Identifiers

RxCUI
856364 856369 856373 856377
UNII
6E8ZO8LRNM

Packaging Origin

Original Packager
true

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 ANDA204852 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (13107-079-01)
  • 500 TABLET in 1 BOTTLE (13107-079-05)
  • 30 TABLET in 1 BOTTLE (13107-079-30)
  • 1000 TABLET in 1 BOTTLE (13107-079-99)
source: ndc

Packages (4)

13107-079-01 100 TABLET in 1 BOTTLE (13107-079-01) 13107-079-05 500 TABLET in 1 BOTTLE (13107-079-05) 13107-079-30 30 TABLET in 1 BOTTLE (13107-079-30) 13107-079-99 1000 TABLET in 1 BOTTLE (13107-079-99)

Ingredients (1)

trazodone hydrochloride (50 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": "db4e6aff-149f-4f16-9512-e81e0c3e6900", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856369", "856373", "856377"], "spl_set_id": ["295e92a9-bcb0-4d53-ba62-e30020e9834b"], "manufacturer_name": ["Aurolife Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13107-079-01)", "package_ndc": "13107-079-01", "marketing_start_date": "20150915"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (13107-079-05)", "package_ndc": "13107-079-05", "marketing_start_date": "20150915"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13107-079-30)", "package_ndc": "13107-079-30", "marketing_start_date": "20150915"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13107-079-99)", "package_ndc": "13107-079-99", "marketing_start_date": "20150915"}], "brand_name": "TRAZODONE HYDROCHLORIDE", "product_id": "13107-079_db4e6aff-149f-4f16-9512-e81e0c3e6900", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "13107-079", "generic_name": "TRAZODONE HYDROCHLORIDE", "labeler_name": "Aurolife Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAZODONE HYDROCHLORIDE", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA204852", "marketing_category": "ANDA", "marketing_start_date": "20150915", "listing_expiration_date": "20261231"}