buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: aiping pharmaceutical, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

buspirone hydrochloride 30 mg/1

Manufacturer
AiPing Pharmaceutical, Inc.

Identifiers & Regulatory

Product NDC 11788-061
Product ID 11788-061_fe9868fd-eb67-48a4-99a3-f25125507e36
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202087
Listing Expiration 2026-12-31
Marketing Start 2025-09-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11788061
Hyphenated Format 11788-061

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
  • 30 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (11788-061-05)
  • 60 TABLET in 1 BOTTLE (11788-061-60)
source: ndc

Packages (2)

11788-061-05 500 TABLET in 1 BOTTLE (11788-061-05) 11788-061-60 60 TABLET in 1 BOTTLE (11788-061-60)

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": "fe9868fd-eb67-48a4-99a3-f25125507e36", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["55810b17-4796-49d0-90e4-8e075d62eda4"], "manufacturer_name": ["AiPing Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (11788-061-05)", "package_ndc": "11788-061-05", "marketing_start_date": "20250926"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (11788-061-60)", "package_ndc": "11788-061-60", "marketing_start_date": "20250926"}], "brand_name": "Buspirone hydrochloride", "product_id": "11788-061_fe9868fd-eb67-48a4-99a3-f25125507e36", "dosage_form": "TABLET", "product_ndc": "11788-061", "generic_name": "Buspirone hydrochloride", "labeler_name": "AiPing Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA202087", "marketing_category": "ANDA", "marketing_start_date": "20250926", "listing_expiration_date": "20261231"}