trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 150 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 50111-450
Product ID 50111-450_3313a8d0-eb39-47a4-b476-0973aad30e02
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071525
Listing Expiration 2026-12-31
Marketing Start 2020-03-11

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50111450
Hyphenated Format 50111-450

Supplemental Identifiers

RxCUI
856364 856373 856377
UPC
0350111450011
UNII
6E8ZO8LRNM

Packaging Origin

Original Packager
true

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 ANDA071525 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50111-450-01)
  • 500 TABLET in 1 BOTTLE (50111-450-02)
source: ndc

Packages (2)

50111-450-01 100 TABLET in 1 BOTTLE (50111-450-01) 50111-450-02 500 TABLET in 1 BOTTLE (50111-450-02)

Ingredients (1)

trazodone hydrochloride (150 mg/1)

Linked Drug Pages (1)

Trazodone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3313a8d0-eb39-47a4-b476-0973aad30e02", "openfda": {"upc": ["0350111450011"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856373", "856377"], "spl_set_id": ["4006d439-e2de-4590-82e9-fc9d56e3ec1b"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50111-450-01)", "package_ndc": "50111-450-01", "marketing_start_date": "20200311"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (50111-450-02)", "package_ndc": "50111-450-02", "marketing_start_date": "20200311"}], "brand_name": "Trazodone Hydrochloride", "product_id": "50111-450_3313a8d0-eb39-47a4-b476-0973aad30e02", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "50111-450", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA071525", "marketing_category": "ANDA", "marketing_start_date": "20200311", "listing_expiration_date": "20261231"}