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 71610-206
Product ID 71610-206_636c7482-d41f-4a26-a55c-183f4169c148
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 71610206
Hyphenated Format 71610-206

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 ANDA078888 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71610-206-30)
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": "636c7482-d41f-4a26-a55c-183f4169c148", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["310c6bea-838b-43e4-87e0-a0050829c242"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71610-206-30)", "package_ndc": "71610-206-30", "marketing_start_date": "20181213"}], "brand_name": "Buspirone hydrochloride", "product_id": "71610-206_636c7482-d41f-4a26-a55c-183f4169c148", "dosage_form": "TABLET", "product_ndc": "71610-206", "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": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20140503", "listing_expiration_date": "20261231"}