buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-799
Product ID 71205-799_864ddd0c-80e5-4b4b-84e9-7d66214464ae
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 71205799
Hyphenated Format 71205-799

Supplemental Identifiers

RxCUI
866094
UPC
0371205799601
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
  • 30 TABLET in 1 BOTTLE (71205-799-30)
  • 60 TABLET in 1 BOTTLE (71205-799-60)
  • 90 TABLET in 1 BOTTLE (71205-799-90)
source: ndc

Packages (3)

71205-799-30 30 TABLET in 1 BOTTLE (71205-799-30) 71205-799-60 60 TABLET in 1 BOTTLE (71205-799-60) 71205-799-90 90 TABLET in 1 BOTTLE (71205-799-90)

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": "864ddd0c-80e5-4b4b-84e9-7d66214464ae", "openfda": {"upc": ["0371205799601"], "unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["864ddd0c-80e5-4b4b-84e9-7d66214464ae"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-799-30)", "package_ndc": "71205-799-30", "marketing_start_date": "20230505"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-799-60)", "package_ndc": "71205-799-60", "marketing_start_date": "20230505"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-799-90)", "package_ndc": "71205-799-90", "marketing_start_date": "20230505"}], "brand_name": "Buspirone Hydrochloride", "product_id": "71205-799_864ddd0c-80e5-4b4b-84e9-7d66214464ae", "dosage_form": "TABLET", "product_ndc": "71205-799", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Proficient Rx LP", "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"}