trazodone hydrochloride
Generic: trazodone hydrochloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
trazodone hydrochloride
Generic Name
trazodone hydrochloride
Labeler
major pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
trazodone hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6868
Product ID
0904-6868_1bfc986d-82a1-4503-8eea-7ebf3186d09d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205253
Listing Expiration
2026-12-31
Marketing Start
2017-12-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046868
Hyphenated Format
0904-6868
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 (0904-6868-61) / 1 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1bfc986d-82a1-4503-8eea-7ebf3186d09d", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856373", "856377"], "spl_set_id": ["8eb85c26-a6cb-4a10-a990-ccc0b20aff08"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6868-61) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6868-61", "marketing_start_date": "20171211"}], "brand_name": "Trazodone Hydrochloride", "product_id": "0904-6868_1bfc986d-82a1-4503-8eea-7ebf3186d09d", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "0904-6868", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Major Pharmaceuticals", "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": "20171211", "listing_expiration_date": "20261231"}