buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: apnar pharma lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler apnar pharma lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 10 mg/1

Manufacturer
APNAR PHARMA LP

Identifiers & Regulatory

Product NDC 24689-907
Product ID 24689-907_19f3df29-51b2-7f8b-e063-6294a90a542f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209696
Listing Expiration 2026-12-31
Marketing Start 2024-06-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24689907
Hyphenated Format 24689-907

Supplemental Identifiers

RxCUI
866018 866083 866090 866094 866111
UPC
0324689921068 0324689921051 0324689781013 0324689785011 0324689921013 0324689907017 0324689933061 0324689907055 0324689781051
UNII
207LT9J9OC

Packaging Origin

Original Packager
true

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 ANDA209696 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (24689-907-01)
  • 500 TABLET in 1 BOTTLE (24689-907-05)
source: ndc

Packages (2)

24689-907-01 100 TABLET in 1 BOTTLE (24689-907-01) 24689-907-05 500 TABLET in 1 BOTTLE (24689-907-05)

Ingredients (1)

buspirone hydrochloride (10 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": "19f3df29-51b2-7f8b-e063-6294a90a542f", "openfda": {"upc": ["0324689921068", "0324689921051", "0324689781013", "0324689785011", "0324689921013", "0324689907017", "0324689933061", "0324689907055", "0324689781051"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["3c115eea-9dbc-4e2c-9d79-42e3388fde5a"], "manufacturer_name": ["APNAR PHARMA LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (24689-907-01)", "package_ndc": "24689-907-01", "marketing_start_date": "20240617"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (24689-907-05)", "package_ndc": "24689-907-05", "marketing_start_date": "20240617"}], "brand_name": "Buspirone Hydrochloride", "product_id": "24689-907_19f3df29-51b2-7f8b-e063-6294a90a542f", "dosage_form": "TABLET", "product_ndc": "24689-907", "generic_name": "Buspirone Hydrochloride", "labeler_name": "APNAR PHARMA LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209696", "marketing_category": "ANDA", "marketing_start_date": "20240617", "listing_expiration_date": "20261231"}