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 7.5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-039
Product ID 82804-039_6760a11b-77e0-4c07-8a29-ac7e483a510d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078246
Listing Expiration 2026-12-31
Marketing Start 2020-02-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804039
Hyphenated Format 82804-039

Supplemental Identifiers

RxCUI
866111
UPC
0382804039609
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 ANDA078246 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (82804-039-20)
  • 30 TABLET in 1 BOTTLE (82804-039-30)
  • 60 TABLET in 1 BOTTLE (82804-039-60)
  • 90 TABLET in 1 BOTTLE (82804-039-90)
source: ndc

Packages (4)

82804-039-20 20 TABLET in 1 BOTTLE (82804-039-20) 82804-039-30 30 TABLET in 1 BOTTLE (82804-039-30) 82804-039-60 60 TABLET in 1 BOTTLE (82804-039-60) 82804-039-90 90 TABLET in 1 BOTTLE (82804-039-90)

Ingredients (1)

buspirone hydrochloride (7.5 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": "6760a11b-77e0-4c07-8a29-ac7e483a510d", "openfda": {"upc": ["0382804039609"], "unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["75b1ae3f-e926-4555-a0e9-50323fc66cb2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (82804-039-20)", "package_ndc": "82804-039-20", "marketing_start_date": "20240227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-039-30)", "package_ndc": "82804-039-30", "marketing_start_date": "20231107"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-039-60)", "package_ndc": "82804-039-60", "marketing_start_date": "20231107"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-039-90)", "package_ndc": "82804-039-90", "marketing_start_date": "20231107"}], "brand_name": "BUSPIRONE HYDROCHLORIDE", "product_id": "82804-039_6760a11b-77e0-4c07-8a29-ac7e483a510d", "dosage_form": "TABLET", "product_ndc": "82804-039", "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": "7.5 mg/1"}], "application_number": "ANDA078246", "marketing_category": "ANDA", "marketing_start_date": "20200221", "listing_expiration_date": "20261231"}