buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 30 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2510
Product ID 71335-2510_822cef27-4fa5-4657-bb0b-4ca16ef37079
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075022
Listing Expiration 2026-12-31
Marketing Start 2004-03-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352510
Hyphenated Format 71335-2510

Supplemental Identifiers

RxCUI
866090
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 ANDA075022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (71335-2510-1)
  • 30 TABLET in 1 BOTTLE (71335-2510-2)
  • 56 TABLET in 1 BOTTLE (71335-2510-3)
  • 90 TABLET in 1 BOTTLE (71335-2510-4)
  • 180 TABLET in 1 BOTTLE (71335-2510-5)
  • 15 TABLET in 1 BOTTLE (71335-2510-6)
  • 120 TABLET in 1 BOTTLE (71335-2510-7)
source: ndc

Packages (7)

71335-2510-1 60 TABLET in 1 BOTTLE (71335-2510-1) 71335-2510-2 30 TABLET in 1 BOTTLE (71335-2510-2) 71335-2510-3 56 TABLET in 1 BOTTLE (71335-2510-3) 71335-2510-4 90 TABLET in 1 BOTTLE (71335-2510-4) 71335-2510-5 180 TABLET in 1 BOTTLE (71335-2510-5) 71335-2510-6 15 TABLET in 1 BOTTLE (71335-2510-6) 71335-2510-7 120 TABLET in 1 BOTTLE (71335-2510-7)

Ingredients (1)

buspirone hydrochloride (30 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": "822cef27-4fa5-4657-bb0b-4ca16ef37079", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866090"], "spl_set_id": ["a8720833-3bbc-4714-b9b8-716c5e55410d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2510-1)", "package_ndc": "71335-2510-1", "marketing_start_date": "20241021"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2510-2)", "package_ndc": "71335-2510-2", "marketing_start_date": "20241021"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (71335-2510-3)", "package_ndc": "71335-2510-3", "marketing_start_date": "20241021"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2510-4)", "package_ndc": "71335-2510-4", "marketing_start_date": "20241021"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2510-5)", "package_ndc": "71335-2510-5", "marketing_start_date": "20241021"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-2510-6)", "package_ndc": "71335-2510-6", "marketing_start_date": "20241021"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2510-7)", "package_ndc": "71335-2510-7", "marketing_start_date": "20241021"}], "brand_name": "Buspirone Hydrochloride", "product_id": "71335-2510_822cef27-4fa5-4657-bb0b-4ca16ef37079", "dosage_form": "TABLET", "product_ndc": "71335-2510", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}