buspirone hcl

Generic: buspirone hydrochloride

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hcl
Generic Name buspirone hydrochloride
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 7.5 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 82868-082
Product ID 82868-082_472049db-f1eb-5e2b-e063-6294a90a2ff8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075521
Listing Expiration 2026-12-31
Marketing Start 2025-06-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82868082
Hyphenated Format 82868-082

Supplemental Identifiers

RxCUI
866111
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 hcl (source: ndc)
Generic Name buspirone hydrochloride (source: ndc)
Application Number ANDA075521 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (82868-082-30)
source: ndc

Packages (1)

82868-082-30 30 TABLET in 1 BOTTLE, PLASTIC (82868-082-30)

Ingredients (1)

buspirone hydrochloride (7.5 mg/1)

Linked Drug Pages (1)

busPIRone HCl ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "472049db-f1eb-5e2b-e063-6294a90a2ff8", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["472049d2-c4d9-5a38-e063-6294a90a5cf1"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-082-30)", "package_ndc": "82868-082-30", "marketing_start_date": "20250619"}], "brand_name": "busPIRone HCl", "product_id": "82868-082_472049db-f1eb-5e2b-e063-6294a90a2ff8", "dosage_form": "TABLET", "product_ndc": "82868-082", "generic_name": "buspirone hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "busPIRone HCl", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA075521", "marketing_category": "ANDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}