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 72162-1927
Product ID 72162-1927_c2768d6f-ba1c-418a-a565-63fcd6b6bce9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078302
Listing Expiration 2026-12-31
Marketing Start 2020-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621927
Hyphenated Format 72162-1927

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 ANDA078302 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (72162-1927-5)
  • 60 TABLET in 1 BOTTLE (72162-1927-6)
source: ndc

Packages (2)

Ingredients (1)

buspirone hydrochloride (30 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c2768d6f-ba1c-418a-a565-63fcd6b6bce9", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866090"], "spl_set_id": ["eb072818-3ca8-430b-91a1-e7fedd37990c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1927-5)", "package_ndc": "72162-1927-5", "marketing_start_date": "20200501"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-1927-6)", "package_ndc": "72162-1927-6", "marketing_start_date": "20200501"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72162-1927_c2768d6f-ba1c-418a-a565-63fcd6b6bce9", "dosage_form": "TABLET", "product_ndc": "72162-1927", "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": "ANDA078302", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}