buspirone hcl

Generic: buspirone hcl

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hcl
Generic Name buspirone hcl
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 7.5 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-458
Product ID 72189-458_2c4dd247-ae5b-fe93-e063-6394a90a937c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202330
Listing Expiration 2026-12-31
Marketing Start 2023-03-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189458
Hyphenated Format 72189-458

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 hcl (source: ndc)
Generic Name buspirone hcl (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 BOTTLE (72189-458-30)
source: ndc

Packages (1)

72189-458-30 30 TABLET in 1 BOTTLE (72189-458-30)

Ingredients (1)

buspirone hydrochloride (7.5 mg/1)

Linked Drug Pages (1)

Buspirone HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4dd247-ae5b-fe93-e063-6394a90a937c", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["f83219c9-8081-fe55-e053-6394a90aa924"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-458-30)", "package_ndc": "72189-458-30", "marketing_start_date": "20230331"}], "brand_name": "Buspirone HCL", "product_id": "72189-458_2c4dd247-ae5b-fe93-e063-6394a90a937c", "dosage_form": "TABLET", "product_ndc": "72189-458", "generic_name": "Buspirone HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone HCL", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA202330", "marketing_category": "ANDA", "marketing_start_date": "20230331", "listing_expiration_date": "20261231"}