buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler epic pharma, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 30 mg/1

Manufacturer
EPIC PHARMA, LLC

Identifiers & Regulatory

Product NDC 42806-665
Product ID 42806-665_ac140e7e-3d5b-4329-8e3e-e21be7417fed
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202087
Listing Expiration 2026-12-31
Marketing Start 2020-06-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806665
Hyphenated Format 42806-665

Supplemental Identifiers

RxCUI
866018 866083 866090 866094
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
  • 60 TABLET in 1 BOTTLE (42806-665-60)
source: ndc

Packages (1)

42806-665-60 60 TABLET in 1 BOTTLE (42806-665-60)

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": "ac140e7e-3d5b-4329-8e3e-e21be7417fed", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["e8f43c66-f8de-419f-9ea9-43ddc4ec0798"], "manufacturer_name": ["EPIC PHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (42806-665-60)", "package_ndc": "42806-665-60", "marketing_start_date": "20200619"}], "brand_name": "Buspirone hydrochloride", "product_id": "42806-665_ac140e7e-3d5b-4329-8e3e-e21be7417fed", "dosage_form": "TABLET", "product_ndc": "42806-665", "generic_name": "Buspirone hydrochloride", "labeler_name": "EPIC PHARMA, LLC", "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": "20200619", "listing_expiration_date": "20261231"}