trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 100 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3756
Product ID 70518-3756_3c580281-e6e4-e007-e063-6294a90a36cf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204852
Listing Expiration 2026-12-31
Marketing Start 2023-06-11

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183756
Hyphenated Format 70518-3756

Supplemental Identifiers

RxCUI
856373
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 ANDA204852 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-3756-0)
source: ndc

Packages (1)

70518-3756-0 30 TABLET in 1 BLISTER PACK (70518-3756-0)

Ingredients (1)

trazodone hydrochloride (100 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": "3c580281-e6e4-e007-e063-6294a90a36cf", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856373"], "spl_set_id": ["fec78f5d-2567-44d3-9f04-1a6913357019"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3756-0)", "package_ndc": "70518-3756-0", "marketing_start_date": "20230611"}], "brand_name": "TRAZODONE HYDROCHLORIDE", "product_id": "70518-3756_3c580281-e6e4-e007-e063-6294a90a36cf", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70518-3756", "generic_name": "TRAZODONE HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAZODONE HYDROCHLORIDE", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA204852", "marketing_category": "ANDA", "marketing_start_date": "20230611", "listing_expiration_date": "20261231"}