buspirone hydrochloride

Generic: buspirone hydrochloride

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

Drug Facts

Product Profile

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

buspirone hydrochloride 10 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-097
Product ID 51655-097_46dddae4-4f92-3775-e063-6394a90a0432
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204582
Listing Expiration 2027-12-31
Marketing Start 2022-08-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655097
Hyphenated Format 51655-097

Supplemental Identifiers

RxCUI
866083
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 ANDA204582 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (51655-097-26)
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-097-52)
  • 180 TABLET in 1 BOTTLE, PLASTIC (51655-097-83)
source: ndc

Packages (3)

51655-097-26 90 TABLET in 1 BOTTLE, PLASTIC (51655-097-26) 51655-097-52 30 TABLET in 1 BOTTLE, PLASTIC (51655-097-52) 51655-097-83 180 TABLET in 1 BOTTLE, PLASTIC (51655-097-83)

Ingredients (1)

buspirone hydrochloride (10 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": "46dddae4-4f92-3775-e063-6394a90a0432", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["1d883a13-4877-c6c7-e063-6294a90a5137"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-097-26)", "package_ndc": "51655-097-26", "marketing_start_date": "20220826"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-097-52)", "package_ndc": "51655-097-52", "marketing_start_date": "20221122"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (51655-097-83)", "package_ndc": "51655-097-83", "marketing_start_date": "20221230"}], "brand_name": "Buspirone Hydrochloride", "product_id": "51655-097_46dddae4-4f92-3775-e063-6394a90a0432", "dosage_form": "TABLET", "product_ndc": "51655-097", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204582", "marketing_category": "ANDA", "marketing_start_date": "20220826", "listing_expiration_date": "20271231"}