buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: advanced rx of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler advanced rx of tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 5 mg/1

Manufacturer
Advanced Rx of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0505
Product ID 80425-0505_30c99025-b56d-aeb3-e063-6294a90a8720
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210907
Listing Expiration 2026-12-31
Marketing Start 2025-03-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250505
Hyphenated Format 80425-0505

Supplemental Identifiers

RxCUI
866094
UNII
207LT9J9OC

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 buspirone hydrochloride (source: ndc)
Generic Name buspirone hydrochloride (source: ndc)
Application Number ANDA210907 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (80425-0505-1)
  • 60 TABLET in 1 BOTTLE, PLASTIC (80425-0505-2)
  • 90 TABLET in 1 BOTTLE, PLASTIC (80425-0505-3)
source: ndc

Packages (3)

80425-0505-1 30 TABLET in 1 BOTTLE, PLASTIC (80425-0505-1) 80425-0505-2 60 TABLET in 1 BOTTLE, PLASTIC (80425-0505-2) 80425-0505-3 90 TABLET in 1 BOTTLE, PLASTIC (80425-0505-3)

Ingredients (1)

buspirone hydrochloride (5 mg/1)

Linked Drug Pages (1)

Buspirone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "30c99025-b56d-aeb3-e063-6294a90a8720", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["30c93022-4126-db8c-e063-6394a90a7579"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (80425-0505-1)", "package_ndc": "80425-0505-1", "marketing_start_date": "20250320"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (80425-0505-2)", "package_ndc": "80425-0505-2", "marketing_start_date": "20250320"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (80425-0505-3)", "package_ndc": "80425-0505-3", "marketing_start_date": "20250320"}], "brand_name": "Buspirone Hydrochloride", "product_id": "80425-0505_30c99025-b56d-aeb3-e063-6294a90a8720", "dosage_form": "TABLET", "product_ndc": "80425-0505", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20250320", "listing_expiration_date": "20261231"}