buspirone hydrochloride
Generic: buspirone hydrochloride
Labeler: accord healthcare inc.Drug Facts
Product Profile
Brand Name
buspirone hydrochloride
Generic Name
buspirone hydrochloride
Labeler
accord healthcare inc.
Dosage Form
TABLET
Routes
Active Ingredients
buspirone hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16729-289
Product ID
16729-289_4092e48b-b3d6-abf3-e063-6394a90afe61
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202557
Listing Expiration
2026-12-31
Marketing Start
2016-12-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16729289
Hyphenated Format
16729-289
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA202557 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (16729-289-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4092e48b-b3d6-abf3-e063-6394a90afe61", "openfda": {"upc": ["0316729289016"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["3da22999-f5fb-49fd-acde-c3006598e985"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (16729-289-12)", "package_ndc": "16729-289-12", "marketing_start_date": "20161215"}], "brand_name": "Buspirone Hydrochloride", "product_id": "16729-289_4092e48b-b3d6-abf3-e063-6394a90afe61", "dosage_form": "TABLET", "product_ndc": "16729-289", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA202557", "marketing_category": "ANDA", "marketing_start_date": "20161215", "listing_expiration_date": "20261231"}