buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5347
Product ID 50090-5347_0676094b-d9ed-4859-a0b6-251a1219840e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202330
Listing Expiration 2027-12-31
Marketing Start 2015-06-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905347
Hyphenated Format 50090-5347

Supplemental Identifiers

RxCUI
866083
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
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-5347-0)
  • 90 TABLET in 1 BOTTLE (50090-5347-1)
  • 180 TABLET in 1 BOTTLE (50090-5347-3)
  • 45 TABLET in 1 BOTTLE (50090-5347-4)
  • 60 TABLET in 1 BOTTLE (50090-5347-5)
source: ndc

Packages (5)

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": "0676094b-d9ed-4859-a0b6-251a1219840e", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["ecdfd79e-7450-40ec-9561-cdda3a043990"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5347-0)", "package_ndc": "50090-5347-0", "marketing_start_date": "20201109"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5347-1)", "package_ndc": "50090-5347-1", "marketing_start_date": "20201109"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-5347-3)", "package_ndc": "50090-5347-3", "marketing_start_date": "20201109"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (50090-5347-4)", "package_ndc": "50090-5347-4", "marketing_start_date": "20201109"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-5347-5)", "package_ndc": "50090-5347-5", "marketing_start_date": "20201109"}], "brand_name": "Buspirone Hydrochloride", "product_id": "50090-5347_0676094b-d9ed-4859-a0b6-251a1219840e", "dosage_form": "TABLET", "product_ndc": "50090-5347", "generic_name": "Buspirone Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202330", "marketing_category": "ANDA", "marketing_start_date": "20150630", "listing_expiration_date": "20271231"}