buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 15 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-025
Product ID 23155-025_5cb34079-0b3b-4c4e-b5a8-bfcdb21d7c3b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204582
Listing Expiration 2026-12-31
Marketing Start 2012-06-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155025
Hyphenated Format 23155-025

Supplemental Identifiers

RxCUI
866018 866083 866090 866094
UNII
207LT9J9OC

Packaging Origin

Original Packager
true

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
  • 15 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-025-01)
  • 500 TABLET in 1 BOTTLE (23155-025-05)
  • 60 TABLET in 1 BOTTLE (23155-025-06)
  • 180 TABLET in 1 BOTTLE (23155-025-08)
source: ndc

Packages (4)

23155-025-01 100 TABLET in 1 BOTTLE (23155-025-01) 23155-025-05 500 TABLET in 1 BOTTLE (23155-025-05) 23155-025-06 60 TABLET in 1 BOTTLE (23155-025-06) 23155-025-08 180 TABLET in 1 BOTTLE (23155-025-08)

Ingredients (1)

buspirone hydrochloride (15 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": "5cb34079-0b3b-4c4e-b5a8-bfcdb21d7c3b", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["4ff72575-bd60-40ce-b3a8-fd92b79af674"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-025-01)", "package_ndc": "23155-025-01", "marketing_start_date": "20180920"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-025-05)", "package_ndc": "23155-025-05", "marketing_start_date": "20180920"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (23155-025-06)", "package_ndc": "23155-025-06", "marketing_start_date": "20150918"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (23155-025-08)", "package_ndc": "23155-025-08", "marketing_start_date": "20180920"}], "brand_name": "Buspirone Hydrochloride", "product_id": "23155-025_5cb34079-0b3b-4c4e-b5a8-bfcdb21d7c3b", "dosage_form": "TABLET", "product_ndc": "23155-025", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA204582", "marketing_category": "ANDA", "marketing_start_date": "20120629", "listing_expiration_date": "20261231"}