buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: oxford pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler oxford pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 15 mg/1

Manufacturer
Oxford Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69584-093
Product ID 69584-093_8c9f66ca-78a9-418c-b11e-ba4391843257
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075388
Listing Expiration 2026-12-31
Marketing Start 2020-07-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69584093
Hyphenated Format 69584-093

Supplemental Identifiers

RxCUI
866018 866083 866090 866094
UPC
0369584093502
UNII
207LT9J9OC

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 buspirone hydrochloride (source: ndc)
Generic Name buspirone hydrochloride (source: ndc)
Application Number ANDA075388 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (69584-093-06)
  • 100 TABLET in 1 BOTTLE (69584-093-10)
  • 500 TABLET in 1 BOTTLE (69584-093-50)
source: ndc

Packages (3)

69584-093-06 60 TABLET in 1 BOTTLE (69584-093-06) 69584-093-10 100 TABLET in 1 BOTTLE (69584-093-10) 69584-093-50 500 TABLET in 1 BOTTLE (69584-093-50)

Ingredients (1)

buspirone hydrochloride (15 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": "8c9f66ca-78a9-418c-b11e-ba4391843257", "openfda": {"upc": ["0369584093502"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["97fcebc1-6615-4b9d-b0f3-6434850f407c"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (69584-093-06)", "package_ndc": "69584-093-06", "marketing_start_date": "20250824"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (69584-093-10)", "package_ndc": "69584-093-10", "marketing_start_date": "20200727"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69584-093-50)", "package_ndc": "69584-093-50", "marketing_start_date": "20200727"}], "brand_name": "Buspirone Hydrochloride", "product_id": "69584-093_8c9f66ca-78a9-418c-b11e-ba4391843257", "dosage_form": "TABLET", "product_ndc": "69584-093", "generic_name": "buspirone hydrochloride", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20261231"}