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 5 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-7714
Product ID 0615-7714_77cbe6b7-dd55-4745-a49e-1e22072beccd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075022
Listing Expiration 2026-12-31
Marketing Start 2002-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06157714
Hyphenated Format 0615-7714

Supplemental Identifiers

RxCUI
866018 866083 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 ANDA075022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BLISTER PACK (0615-7714-05)
  • 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7714-30) / 5 TABLET in 1 BLISTER PACK
  • 30 TABLET in 1 BLISTER PACK (0615-7714-39)
source: ndc

Packages (3)

Ingredients (1)

buspirone hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "77cbe6b7-dd55-4745-a49e-1e22072beccd", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866094"], "spl_set_id": ["72bff09c-826e-4394-a7e7-41d56ce9605b"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BLISTER PACK (0615-7714-05)", "package_ndc": "0615-7714-05", "marketing_start_date": "20221121"}, {"sample": false, "description": "6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7714-30)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "0615-7714-30", "marketing_start_date": "20120423"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-7714-39)", "package_ndc": "0615-7714-39", "marketing_start_date": "20120423"}], "brand_name": "Buspirone Hydrochloride", "product_id": "0615-7714_77cbe6b7-dd55-4745-a49e-1e22072beccd", "dosage_form": "TABLET", "product_ndc": "0615-7714", "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": "5 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20020228", "listing_expiration_date": "20261231"}