trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: granules pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

trazodone hydrochloride 50 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-231
Product ID 70010-231_30d886ac-9a27-a66f-e063-6394a90aa2b1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218988
Listing Expiration 2026-12-31
Marketing Start 2024-08-09

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70010231
Hyphenated Format 70010-231

Supplemental Identifiers

RxCUI
856364 856369 856373 856377
UPC
0370010231030 0370010232037 0370010234031 0370010233034
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 ANDA218988 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70010-231-01)
  • 30 TABLET in 1 BOTTLE (70010-231-03)
  • 500 TABLET in 1 BOTTLE (70010-231-05)
  • 1000 TABLET in 1 BOTTLE (70010-231-10)
source: ndc

Packages (4)

70010-231-01 100 TABLET in 1 BOTTLE (70010-231-01) 70010-231-03 30 TABLET in 1 BOTTLE (70010-231-03) 70010-231-05 500 TABLET in 1 BOTTLE (70010-231-05) 70010-231-10 1000 TABLET in 1 BOTTLE (70010-231-10)

Ingredients (1)

trazodone hydrochloride (50 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": "30d886ac-9a27-a66f-e063-6394a90aa2b1", "openfda": {"upc": ["0370010231030", "0370010232037", "0370010234031", "0370010233034"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856369", "856373", "856377"], "spl_set_id": ["5bc5f266-6c0e-4b9a-b6e0-ea694928b948"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70010-231-01)", "package_ndc": "70010-231-01", "marketing_start_date": "20240809"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70010-231-03)", "package_ndc": "70010-231-03", "marketing_start_date": "20240809"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70010-231-05)", "package_ndc": "70010-231-05", "marketing_start_date": "20240809"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70010-231-10)", "package_ndc": "70010-231-10", "marketing_start_date": "20241001"}], "brand_name": "Trazodone Hydrochloride", "product_id": "70010-231_30d886ac-9a27-a66f-e063-6394a90aa2b1", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70010-231", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA218988", "marketing_category": "ANDA", "marketing_start_date": "20240809", "listing_expiration_date": "20261231"}