trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler zydus lifesciences limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 50 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1128
Product ID 70771-1128_0b9d3b91-26ed-477b-a88e-2d6a76fedabf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205253
Marketing Start 2017-12-11
Marketing End 2028-12-31

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711128
Hyphenated Format 70771-1128

Supplemental Identifiers

RxCUI
856364 856369 856373 856377
UPC
0368382808011 0368382609014
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 ANDA205253 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (70771-1128-0)
  • 100 TABLET in 1 BOTTLE (70771-1128-1)
  • 30 TABLET in 1 BOTTLE (70771-1128-3)
  • 10 BLISTER PACK in 1 CARTON (70771-1128-4) / 10 TABLET in 1 BLISTER PACK (70771-1128-2)
  • 500 TABLET in 1 BOTTLE (70771-1128-5)
  • 90 TABLET in 1 BOTTLE (70771-1128-9)
source: ndc

Packages (6)

70771-1128-0 1000 TABLET in 1 BOTTLE (70771-1128-0) 70771-1128-1 100 TABLET in 1 BOTTLE (70771-1128-1) 70771-1128-3 30 TABLET in 1 BOTTLE (70771-1128-3) 70771-1128-4 10 BLISTER PACK in 1 CARTON (70771-1128-4) / 10 TABLET in 1 BLISTER PACK (70771-1128-2) 70771-1128-5 500 TABLET in 1 BOTTLE (70771-1128-5) 70771-1128-9 90 TABLET in 1 BOTTLE (70771-1128-9)

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": "0b9d3b91-26ed-477b-a88e-2d6a76fedabf", "openfda": {"upc": ["0368382808011", "0368382609014"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856369", "856373", "856377"], "spl_set_id": ["43d4be17-5fae-4326-a5c4-9e25e2db6a43"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70771-1128-0)", "package_ndc": "70771-1128-0", "marketing_end_date": "20281231", "marketing_start_date": "20171211"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1128-1)", "package_ndc": "70771-1128-1", "marketing_end_date": "20281231", "marketing_start_date": "20171211"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70771-1128-3)", "package_ndc": "70771-1128-3", "marketing_end_date": "20281231", "marketing_start_date": "20171211"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1128-4)  / 10 TABLET in 1 BLISTER PACK (70771-1128-2)", "package_ndc": "70771-1128-4", "marketing_end_date": "20281231", "marketing_start_date": "20171211"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1128-5)", "package_ndc": "70771-1128-5", "marketing_end_date": "20281231", "marketing_start_date": "20171211"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70771-1128-9)", "package_ndc": "70771-1128-9", "marketing_end_date": "20281231", "marketing_start_date": "20171211"}], "brand_name": "Trazodone Hydrochloride", "product_id": "70771-1128_0b9d3b91-26ed-477b-a88e-2d6a76fedabf", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "70771-1128", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "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_end_date": "20281231", "marketing_start_date": "20171211"}