buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 10 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-0054
Product ID 0093-0054_f2a05d58-ca70-4b89-aa19-6b63e85a57a5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075022
Listing Expiration 2026-12-31
Marketing Start 2002-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00930054
Hyphenated Format 0093-0054

Supplemental Identifiers

RxCUI
866018 866083 866090 866094
UPC
0300930054013
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 ANDA075022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0093-0054-01)
  • 500 TABLET in 1 BOTTLE (0093-0054-05)
source: ndc

Packages (2)

0093-0054-01 100 TABLET in 1 BOTTLE (0093-0054-01) 0093-0054-05 500 TABLET in 1 BOTTLE (0093-0054-05)

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": "f2a05d58-ca70-4b89-aa19-6b63e85a57a5", "openfda": {"upc": ["0300930054013"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["6fac36b4-b223-479e-913f-f8c9cdb9e119"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-0054-01)", "package_ndc": "0093-0054-01", "marketing_start_date": "20020228"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0093-0054-05)", "package_ndc": "0093-0054-05", "marketing_start_date": "20020301"}], "brand_name": "Buspirone Hydrochloride", "product_id": "0093-0054_f2a05d58-ca70-4b89-aa19-6b63e85a57a5", "dosage_form": "TABLET", "product_ndc": "0093-0054", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20020228", "listing_expiration_date": "20261231"}