buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

buspirone hydrochloride 5 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7952
Product ID 68788-7952_c8cdb1c5-8415-43ca-9bdd-1bb194a2bc0f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210907
Listing Expiration 2026-12-31
Marketing Start 2021-07-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887952
Hyphenated Format 68788-7952

Supplemental Identifiers

RxCUI
866094
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 ANDA210907 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (68788-7952-1)
  • 30 TABLET in 1 BOTTLE, PLASTIC (68788-7952-3)
  • 60 TABLET in 1 BOTTLE, PLASTIC (68788-7952-6)
  • 90 TABLET in 1 BOTTLE, PLASTIC (68788-7952-9)
source: ndc

Packages (4)

68788-7952-1 100 TABLET in 1 BOTTLE, PLASTIC (68788-7952-1) 68788-7952-3 30 TABLET in 1 BOTTLE, PLASTIC (68788-7952-3) 68788-7952-6 60 TABLET in 1 BOTTLE, PLASTIC (68788-7952-6) 68788-7952-9 90 TABLET in 1 BOTTLE, PLASTIC (68788-7952-9)

Ingredients (1)

buspirone hydrochloride (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": "c8cdb1c5-8415-43ca-9bdd-1bb194a2bc0f", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["824c80e6-d508-405f-8a4f-2f10df5a9dc8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (68788-7952-1)", "package_ndc": "68788-7952-1", "marketing_start_date": "20210709"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68788-7952-3)", "package_ndc": "68788-7952-3", "marketing_start_date": "20210709"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (68788-7952-6)", "package_ndc": "68788-7952-6", "marketing_start_date": "20210709"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (68788-7952-9)", "package_ndc": "68788-7952-9", "marketing_start_date": "20210709"}], "brand_name": "Buspirone Hydrochloride", "product_id": "68788-7952_c8cdb1c5-8415-43ca-9bdd-1bb194a2bc0f", "dosage_form": "TABLET", "product_ndc": "68788-7952", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20210709", "listing_expiration_date": "20261231"}