buspirone hydrochloride
Generic: buspirone hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
buspirone hydrochloride
Generic Name
buspirone hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
buspirone hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7652
Product ID
50090-7652_2bc9354b-de6e-48d7-b001-c1179befd893
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210907
Listing Expiration
2026-12-31
Marketing Start
2023-10-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907652
Hyphenated Format
50090-7652
Supplemental Identifiers
RxCUI
UNII
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
ANDA210907 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (50090-7652-0)
- 90 TABLET in 1 BOTTLE (50090-7652-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2bc9354b-de6e-48d7-b001-c1179befd893", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866090"], "spl_set_id": ["48b4e52d-d4c4-4d24-a0ac-24316371cef0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7652-0)", "package_ndc": "50090-7652-0", "marketing_start_date": "20250909"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7652-1)", "package_ndc": "50090-7652-1", "marketing_start_date": "20250909"}], "brand_name": "Buspirone Hydrochloride", "product_id": "50090-7652_2bc9354b-de6e-48d7-b001-c1179befd893", "dosage_form": "TABLET", "product_ndc": "50090-7652", "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": "30 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20231017", "listing_expiration_date": "20261231"}