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 5 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-203
Product ID 71610-203_3837aaad-61a9-4f61-ac1a-022302c51d21
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075022
Listing Expiration 2026-12-31
Marketing Start 2002-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610203
Hyphenated Format 71610-203

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 ANDA075022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (71610-203-53)
  • 90 TABLET in 1 BOTTLE (71610-203-60)
  • 180 TABLET in 1 BOTTLE (71610-203-80)
source: ndc

Packages (3)

71610-203-53 60 TABLET in 1 BOTTLE (71610-203-53) 71610-203-60 90 TABLET in 1 BOTTLE (71610-203-60) 71610-203-80 180 TABLET in 1 BOTTLE (71610-203-80)

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": "3837aaad-61a9-4f61-ac1a-022302c51d21", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["efa03f52-430e-455a-bdca-7f9d422b7b19"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-203-53)", "package_ndc": "71610-203-53", "marketing_start_date": "20181203"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-203-60)", "package_ndc": "71610-203-60", "marketing_start_date": "20181203"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-203-80)", "package_ndc": "71610-203-80", "marketing_start_date": "20181203"}], "brand_name": "Buspirone Hydrochloride", "product_id": "71610-203_3837aaad-61a9-4f61-ac1a-022302c51d21", "dosage_form": "TABLET", "product_ndc": "71610-203", "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": "5 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20020228", "listing_expiration_date": "20261231"}