buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 15 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-183
Product ID 71610-183_0e7eed66-f0af-469e-ad79-8d442af82177
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075022
Listing Expiration 2026-12-31
Marketing Start 2002-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610183
Hyphenated Format 71610-183

Supplemental Identifiers

RxCUI
866018
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 ANDA075022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (71610-183-60)
source: ndc

Packages (1)

Ingredients (1)

buspirone hydrochloride (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e7eed66-f0af-469e-ad79-8d442af82177", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["b7e3a98c-9ec5-4c21-9218-0d53a555a75c"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-183-60)", "package_ndc": "71610-183-60", "marketing_start_date": "20181031"}], "brand_name": "Buspirone Hydrochloride", "product_id": "71610-183_0e7eed66-f0af-469e-ad79-8d442af82177", "dosage_form": "TABLET", "product_ndc": "71610-183", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20020301", "listing_expiration_date": "20261231"}