trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler avpak
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 150 mg/1

Manufacturer
AvPAK

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
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268776
Hyphenated Format 50268-776

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
  • 50 BLISTER PACK in 1 BOX (50268-776-15) / 1 TABLET in 1 BLISTER PACK (50268-776-11)
source: ndc

Packages (1)

Ingredients (1)

trazodone hydrochloride (150 mg/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"}