buspirone hydrochloride
Generic: buspirone hydrochloride
Labeler: safecor health, llcDrug Facts
Product Profile
Brand Name
buspirone hydrochloride
Generic Name
buspirone hydrochloride
Labeler
safecor health, llc
Dosage Form
TABLET
Routes
Active Ingredients
buspirone hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
48433-012
Product ID
48433-012_4b433e49-a0b8-2f27-e063-6294a90af1b9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076008
Listing Expiration
2027-12-31
Marketing Start
2026-02-04
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
48433012
Hyphenated Format
48433-012
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
ANDA076008 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (48433-012-20) / 1 TABLET in 1 BLISTER PACK (48433-012-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b433e49-a0b8-2f27-e063-6294a90af1b9", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["ebda05ee-d895-4636-bc28-d393e69c91b3"], "manufacturer_name": ["Safecor Health, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (48433-012-20) / 1 TABLET in 1 BLISTER PACK (48433-012-01)", "package_ndc": "48433-012-20", "marketing_start_date": "20260204"}], "brand_name": "Buspirone Hydrochloride", "product_id": "48433-012_4b433e49-a0b8-2f27-e063-6294a90af1b9", "dosage_form": "TABLET", "product_ndc": "48433-012", "generic_name": "buspirone hydrochloride", "labeler_name": "Safecor Health, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076008", "marketing_category": "ANDA", "marketing_start_date": "20260204", "listing_expiration_date": "20271231"}