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 150 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2180
Product ID 70518-2180_49db46f7-1ae9-7c94-e063-6294a90a94e3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205253
Listing Expiration 2027-12-31
Marketing Start 2019-07-01

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182180
Hyphenated Format 70518-2180

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, PLASTIC (70518-2180-2)
source: ndc

Packages (1)

70518-2180-2 30 TABLET in 1 BOTTLE, PLASTIC (70518-2180-2)

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": "49db46f7-1ae9-7c94-e063-6294a90a94e3", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["2863317d-657b-4dc6-81fb-b7158ea03498"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-2180-2)", "package_ndc": "70518-2180-2", "marketing_start_date": "20251017"}], "brand_name": "Trazodone Hydrochloride", "product_id": "70518-2180_49db46f7-1ae9-7c94-e063-6294a90a94e3", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2180", "generic_name": "Trazodone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20190701", "listing_expiration_date": "20271231"}