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 15 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6971
Product ID
50090-6971_925f0625-454c-4646-81ca-b9b07c67a576
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210907
Listing Expiration
2026-12-31
Marketing Start
2019-11-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906971
Hyphenated Format
50090-6971
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
- 15 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (50090-6971-1)
- 90 TABLET in 1 BOTTLE (50090-6971-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "925f0625-454c-4646-81ca-b9b07c67a576", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["bce96786-4d9a-460e-8d92-9908ea2af07a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6971-1)", "package_ndc": "50090-6971-1", "marketing_start_date": "20231221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6971-3)", "package_ndc": "50090-6971-3", "marketing_start_date": "20231221"}], "brand_name": "Buspirone Hydrochloride", "product_id": "50090-6971_925f0625-454c-4646-81ca-b9b07c67a576", "dosage_form": "TABLET", "product_ndc": "50090-6971", "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": "15 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20191114", "listing_expiration_date": "20261231"}