buspirone hydrochloride

Generic: buspirone hydrochloride

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

Drug Facts

Product Profile

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

buspirone hydrochloride 10 mg/1

Manufacturer
Radha Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 77771-236
Product ID 77771-236_3f66a40c-b9b2-06d4-e063-6294a90a9dda
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202087
Listing Expiration 2026-12-31
Marketing Start 2025-09-18

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 77771236
Hyphenated Format 77771-236

Supplemental Identifiers

RxCUI
866018 866083 866090 866094 866111
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 ANDA202087 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (77771-236-01)
  • 500 TABLET in 1 BOTTLE (77771-236-05)
source: ndc

Packages (2)

77771-236-01 100 TABLET in 1 BOTTLE (77771-236-01) 77771-236-05 500 TABLET in 1 BOTTLE (77771-236-05)

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": "3f66a40c-b9b2-06d4-e063-6294a90a9dda", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["3f66a3fe-9d73-180c-e063-6394a90aacca"], "manufacturer_name": ["Radha Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (77771-236-01)", "package_ndc": "77771-236-01", "marketing_start_date": "20250918"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (77771-236-05)", "package_ndc": "77771-236-05", "marketing_start_date": "20250918"}], "brand_name": "Buspirone hydrochloride", "product_id": "77771-236_3f66a40c-b9b2-06d4-e063-6294a90a9dda", "dosage_form": "TABLET", "product_ndc": "77771-236", "generic_name": "Buspirone hydrochloride", "labeler_name": "Radha Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202087", "marketing_category": "ANDA", "marketing_start_date": "20250918", "listing_expiration_date": "20261231"}