Trazodone Hydrochloride

Generic: Trazodone Hydrochloride

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Trazodone Hydrochloride
Generic Name Trazodone Hydrochloride
Labeler REMEDYREPACK INC.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

TRAZODONE HYDROCHLORIDE 50 mg/1

Identifiers & Regulatory

Product NDC 70518-2929
Product ID 70518-2929_408283bb-9905-3c52-e063-6394a90a853e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071523
Listing Expiration 2026-12-31
Marketing Start 2020-10-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182929
Hyphenated Format 70518-2929

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 ANDA071523 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-2929-0)
  • 30 TABLET in 1 BOTTLE, PLASTIC (70518-2929-7)
source: ndc

Packages (2)

70518-2929-0 30 TABLET in 1 BLISTER PACK (70518-2929-0) 70518-2929-7 30 TABLET in 1 BOTTLE, PLASTIC (70518-2929-7)

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": "408283bb-9905-3c52-e063-6394a90a853e", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856377"], "spl_set_id": ["38e9820a-6edc-4bf5-b5e4-034b9e48b583"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2929-0)", "package_ndc": "70518-2929-0", "marketing_start_date": "20201031"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-2929-7)", "package_ndc": "70518-2929-7", "marketing_start_date": "20241205"}], "brand_name": "Trazodone Hydrochloride", "product_id": "70518-2929_408283bb-9905-3c52-e063-6394a90a853e", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2929", "generic_name": "Trazodone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA071523", "marketing_category": "ANDA", "marketing_start_date": "20201031", "listing_expiration_date": "20261231"}