trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 50 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-443
Product ID 60687-443_4121a0e8-9204-0334-e063-6294a90aa532
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205253
Listing Expiration 2026-12-31
Marketing Start 2019-03-14

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687443
Hyphenated Format 60687-443

Supplemental Identifiers

RxCUI
856364 856373 856377
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
  • 100 BLISTER PACK in 1 CARTON (60687-443-01) / 1 TABLET in 1 BLISTER PACK (60687-443-11)
source: ndc

Packages (1)

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": "4121a0e8-9204-0334-e063-6294a90aa532", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856373", "856377"], "spl_set_id": ["094ca37b-3ae2-4889-9536-e7e5f20e3105"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-443-01)  / 1 TABLET in 1 BLISTER PACK (60687-443-11)", "package_ndc": "60687-443-01", "marketing_start_date": "20190314"}], "brand_name": "Trazodone Hydrochloride", "product_id": "60687-443_4121a0e8-9204-0334-e063-6294a90aa532", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "60687-443", "generic_name": "Trazodone Hydrochloride", "labeler_name": "American Health Packaging", "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": "20190314", "listing_expiration_date": "20261231"}