buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 7.5 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8434
Product ID 0615-8434_53468e3e-9a6e-4f97-b3f4-8e73e633a97e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202330
Listing Expiration 2026-12-31
Marketing Start 2017-02-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06158434
Hyphenated Format 0615-8434

Supplemental Identifiers

RxCUI
866111
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 ANDA202330 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (0615-8434-39)
source: ndc

Packages (1)

0615-8434-39 30 TABLET in 1 BLISTER PACK (0615-8434-39)

Ingredients (1)

buspirone hydrochloride (7.5 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": "53468e3e-9a6e-4f97-b3f4-8e73e633a97e", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["da6f4a74-a71e-4ccc-af2c-8de29e909c3b"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8434-39)", "package_ndc": "0615-8434-39", "marketing_start_date": "20220714"}], "brand_name": "Buspirone Hydrochloride", "product_id": "0615-8434_53468e3e-9a6e-4f97-b3f4-8e73e633a97e", "dosage_form": "TABLET", "product_ndc": "0615-8434", "generic_name": "Buspirone Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA202330", "marketing_category": "ANDA", "marketing_start_date": "20170217", "listing_expiration_date": "20261231"}