buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: safecor health, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler safecor health, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 30 mg/1

Manufacturer
Safecor Health, LLC

Identifiers & Regulatory

Product NDC 48433-014
Product ID 48433-014_4b433e49-a0b8-2f27-e063-6294a90af1b9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076008
Listing Expiration 2027-12-31
Marketing Start 2026-02-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 48433014
Hyphenated Format 48433-014

Supplemental Identifiers

RxCUI
866018 866083 866090 866094
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 ANDA076008 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (48433-014-20) / 1 TABLET in 1 BLISTER PACK (48433-014-01)
source: ndc

Packages (1)

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": "4b433e49-a0b8-2f27-e063-6294a90af1b9", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["ebda05ee-d895-4636-bc28-d393e69c91b3"], "manufacturer_name": ["Safecor Health, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (48433-014-20)  / 1 TABLET in 1 BLISTER PACK (48433-014-01)", "package_ndc": "48433-014-20", "marketing_start_date": "20260204"}], "brand_name": "Buspirone Hydrochloride", "product_id": "48433-014_4b433e49-a0b8-2f27-e063-6294a90af1b9", "dosage_form": "TABLET", "product_ndc": "48433-014", "generic_name": "buspirone hydrochloride", "labeler_name": "Safecor Health, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA076008", "marketing_category": "ANDA", "marketing_start_date": "20260204", "listing_expiration_date": "20271231"}