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 71610-266
Product ID 71610-266_bbf54820-016c-4a8b-b50c-1ce5e26f4c3e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078888
Listing Expiration 2026-12-31
Marketing Start 2014-05-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610266
Hyphenated Format 71610-266

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 ANDA078888 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (71610-266-53)
  • 90 TABLET in 1 BOTTLE (71610-266-60)
  • 180 TABLET in 1 BOTTLE (71610-266-80)
source: ndc

Packages (3)

71610-266-53 60 TABLET in 1 BOTTLE (71610-266-53) 71610-266-60 90 TABLET in 1 BOTTLE (71610-266-60) 71610-266-80 180 TABLET in 1 BOTTLE (71610-266-80)

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": "bbf54820-016c-4a8b-b50c-1ce5e26f4c3e", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["7f6986a8-59dc-4dc3-bac0-b38cfc689f8f"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-266-53)", "package_ndc": "71610-266-53", "marketing_start_date": "20190425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-266-60)", "package_ndc": "71610-266-60", "marketing_start_date": "20190425"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-266-80)", "package_ndc": "71610-266-80", "marketing_start_date": "20190425"}], "brand_name": "Buspirone hydrochloride", "product_id": "71610-266_bbf54820-016c-4a8b-b50c-1ce5e26f4c3e", "dosage_form": "TABLET", "product_ndc": "71610-266", "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": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20140503", "listing_expiration_date": "20261231"}