trazodone hydrochloride
Generic: trazodone hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
trazodone hydrochloride
Generic Name
trazodone hydrochloride
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
trazodone hydrochloride 50 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687443
Hyphenated Format
60687-443
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (60687-443-01) / 1 TABLET in 1 BLISTER PACK (60687-443-11)
Packages (1)
Ingredients (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"}