trazodone hydrochloride
Generic: trazodone hydrochloride
Labeler: avpakDrug Facts
Product Profile
Brand Name
trazodone hydrochloride
Generic Name
trazodone hydrochloride
Labeler
avpak
Dosage Form
TABLET
Routes
Active Ingredients
trazodone hydrochloride 150 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50268-776
Product ID
50268-776_4836a55b-859d-c6d2-e063-6294a90ae94d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205253
Listing Expiration
2027-12-31
Marketing Start
2020-02-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268776
Hyphenated Format
50268-776
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
- 150 mg/1
Packaging
- 50 BLISTER PACK in 1 BOX (50268-776-15) / 1 TABLET in 1 BLISTER PACK (50268-776-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4836a55b-859d-c6d2-e063-6294a90ae94d", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364"], "spl_set_id": ["9f1c2bf1-5204-7306-e053-2a95a90a9903"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-776-15) / 1 TABLET in 1 BLISTER PACK (50268-776-11)", "package_ndc": "50268-776-15", "marketing_start_date": "20200221"}], "brand_name": "Trazodone Hydrochloride", "product_id": "50268-776_4836a55b-859d-c6d2-e063-6294a90ae94d", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "50268-776", "generic_name": "Trazodone Hydrochloride", "labeler_name": "AvPAK", "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": "20200221", "listing_expiration_date": "20271231"}