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 30 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-964
Product ID 82804-964_1521109d-8386-472f-9483-f1fe9f7ed152
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078302
Listing Expiration 2027-12-31
Marketing Start 2020-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804964
Hyphenated Format 82804-964

Supplemental Identifiers

RxCUI
866018 866083 866090 866094
UPC
0382804962303 0382804961306
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 ANDA078302 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (82804-964-00)
  • 1000 TABLET in 1 BOTTLE (82804-964-11)
  • 30 TABLET in 1 BOTTLE (82804-964-30)
  • 500 TABLET in 1 BOTTLE (82804-964-55)
  • 60 TABLET in 1 BOTTLE (82804-964-60)
  • 120 TABLET in 1 BOTTLE (82804-964-72)
  • 90 TABLET in 1 BOTTLE (82804-964-90)
source: ndc

Packages (7)

82804-964-00 100 TABLET in 1 BOTTLE (82804-964-00) 82804-964-11 1000 TABLET in 1 BOTTLE (82804-964-11) 82804-964-30 30 TABLET in 1 BOTTLE (82804-964-30) 82804-964-55 500 TABLET in 1 BOTTLE (82804-964-55) 82804-964-60 60 TABLET in 1 BOTTLE (82804-964-60) 82804-964-72 120 TABLET in 1 BOTTLE (82804-964-72) 82804-964-90 90 TABLET in 1 BOTTLE (82804-964-90)

Ingredients (1)

buspirone hydrochloride (30 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": "1521109d-8386-472f-9483-f1fe9f7ed152", "openfda": {"upc": ["0382804962303", "0382804961306"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["1521109d-8386-472f-9483-f1fe9f7ed152"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82804-964-00)", "package_ndc": "82804-964-00", "marketing_start_date": "20260112"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-964-11)", "package_ndc": "82804-964-11", "marketing_start_date": "20260112"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-964-30)", "package_ndc": "82804-964-30", "marketing_start_date": "20260112"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-964-55)", "package_ndc": "82804-964-55", "marketing_start_date": "20260112"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-964-60)", "package_ndc": "82804-964-60", "marketing_start_date": "20260112"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-964-72)", "package_ndc": "82804-964-72", "marketing_start_date": "20260112"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-964-90)", "package_ndc": "82804-964-90", "marketing_start_date": "20260112"}], "brand_name": "Buspirone Hydrochloride", "product_id": "82804-964_1521109d-8386-472f-9483-f1fe9f7ed152", "dosage_form": "TABLET", "product_ndc": "82804-964", "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": "30 mg/1"}], "application_number": "ANDA078302", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20271231"}