trazodone hydrochloride

Generic: trazodone hydrochloride

Labeler: torrent pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trazodone hydrochloride
Generic Name trazodone hydrochloride
Labeler torrent pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trazodone hydrochloride 150 mg/1

Manufacturer
Torrent Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 13668-332
Product ID 13668-332_bc2a4de4-8b05-4bb8-bf92-b7f5daa0a6f3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202180
Listing Expiration 2027-12-31
Marketing Start 2013-11-27

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 13668332
Hyphenated Format 13668-332

Supplemental Identifiers

RxCUI
856364 856369 856373 856377
UPC
0313668332308 0313668331301 0313668330304 0313668333015
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 ANDA202180 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (13668-332-01)
  • 500 TABLET in 1 BOTTLE (13668-332-05)
  • 1000 TABLET in 1 BOTTLE (13668-332-10)
  • 30 TABLET in 1 BOTTLE (13668-332-30)
source: ndc

Packages (4)

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": "bc2a4de4-8b05-4bb8-bf92-b7f5daa0a6f3", "openfda": {"upc": ["0313668332308", "0313668331301", "0313668330304", "0313668333015"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856369", "856373", "856377"], "spl_set_id": ["1510cf89-a2ec-4ed5-80cb-bae84f9ec0a7"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13668-332-01)", "package_ndc": "13668-332-01", "marketing_start_date": "20131127"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (13668-332-05)", "package_ndc": "13668-332-05", "marketing_start_date": "20131127"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13668-332-10)", "package_ndc": "13668-332-10", "marketing_start_date": "20131127"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13668-332-30)", "package_ndc": "13668-332-30", "marketing_start_date": "20131127"}], "brand_name": "Trazodone Hydrochloride", "product_id": "13668-332_bc2a4de4-8b05-4bb8-bf92-b7f5daa0a6f3", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "13668-332", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA202180", "marketing_category": "ANDA", "marketing_start_date": "20131127", "listing_expiration_date": "20271231"}