buspirone hydrochloride
Generic: buspirone hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
buspirone hydrochloride
Generic Name
buspirone hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
buspirone hydrochloride 15 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-2413
Product ID
63629-2413_3df8d041-a935-49ff-8545-e53e6cfa033e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075388
Listing Expiration
2026-12-31
Marketing Start
2020-07-27
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636292413
Hyphenated Format
63629-2413
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
ANDA075388 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 15 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (63629-2413-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3df8d041-a935-49ff-8545-e53e6cfa033e", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["65c69118-36bb-4f0d-9669-b52556056ec5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-2413-1)", "package_ndc": "63629-2413-1", "marketing_start_date": "20210224"}], "brand_name": "Buspirone Hydrochloride", "product_id": "63629-2413_3df8d041-a935-49ff-8545-e53e6cfa033e", "dosage_form": "TABLET", "product_ndc": "63629-2413", "generic_name": "buspirone hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20261231"}