buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

buspirone hydrochloride 10 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3881
Product ID 68071-3881_3b4200bf-b66d-6936-e063-6394a90a6f19
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 680713881
Hyphenated Format 68071-3881

Supplemental Identifiers

RxCUI
866083
UPC
0368071388169
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
  • 10 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (68071-3881-6)
source: ndc

Packages (1)

Ingredients (1)

buspirone hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b4200bf-b66d-6936-e063-6394a90a6f19", "openfda": {"upc": ["0368071388169"], "unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["3b41fd76-c3cc-77f0-e063-6294a90aa778"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3881-6)", "package_ndc": "68071-3881-6", "marketing_start_date": "20250731"}], "brand_name": "Buspirone Hydrochloride", "product_id": "68071-3881_3b4200bf-b66d-6936-e063-6394a90a6f19", "dosage_form": "TABLET", "product_ndc": "68071-3881", "generic_name": "Buspirone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20020228", "listing_expiration_date": "20261231"}