nefazodone hydrochloride

Generic: nefazodone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nefazodone hydrochloride
Generic Name nefazodone hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nefazodone hydrochloride 150 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-7046
Product ID 63629-7046_8962e4a7-1e27-4a03-ab51-34fc4f9c6847
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076037
Listing Expiration 2026-12-31
Marketing Start 2003-09-16

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636297046
Hyphenated Format 63629-7046

Supplemental Identifiers

RxCUI
1098666
UNII
27X63J94GR

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 nefazodone hydrochloride (source: ndc)
Generic Name nefazodone hydrochloride (source: ndc)
Application Number ANDA076037 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63629-7046-1)
  • 120 TABLET in 1 BOTTLE (63629-7046-2)
  • 28 TABLET in 1 BOTTLE (63629-7046-3)
  • 60 TABLET in 1 BOTTLE (63629-7046-4)
source: ndc

Packages (4)

Ingredients (1)

nefazodone hydrochloride (150 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8962e4a7-1e27-4a03-ab51-34fc4f9c6847", "openfda": {"unii": ["27X63J94GR"], "rxcui": ["1098666"], "spl_set_id": ["0bd4c34a-4f43-4c84-8b98-1d074cba97d5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-7046-1)", "package_ndc": "63629-7046-1", "marketing_start_date": "20220208"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (63629-7046-2)", "package_ndc": "63629-7046-2", "marketing_start_date": "20161018"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (63629-7046-3)", "package_ndc": "63629-7046-3", "marketing_start_date": "20220208"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-7046-4)", "package_ndc": "63629-7046-4", "marketing_start_date": "20220208"}], "brand_name": "Nefazodone Hydrochloride", "product_id": "63629-7046_8962e4a7-1e27-4a03-ab51-34fc4f9c6847", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "63629-7046", "generic_name": "Nefazodone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nefazodone Hydrochloride", "active_ingredients": [{"name": "NEFAZODONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA076037", "marketing_category": "ANDA", "marketing_start_date": "20030916", "listing_expiration_date": "20261231"}