buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 5 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 61919-166
Product ID 61919-166_47e15246-5edb-3524-e063-6294a90a3fd4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202557
Listing Expiration 2027-12-31
Marketing Start 2019-07-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61919166
Hyphenated Format 61919-166

Supplemental Identifiers

RxCUI
866094
UNII
207LT9J9OC

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (61919-166-60)
source: ndc

Packages (1)

61919-166-60 60 TABLET in 1 BOTTLE (61919-166-60)

Ingredients (1)

buspirone hydrochloride (5 mg/1)

Linked Drug Pages (1)

BUSPIRONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47e15246-5edb-3524-e063-6294a90a3fd4", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["8e9c0553-c994-f54a-e053-2a95a90a6fa3"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (61919-166-60)", "package_ndc": "61919-166-60", "marketing_start_date": "20190726"}], "brand_name": "BUSPIRONE HYDROCHLORIDE", "product_id": "61919-166_47e15246-5edb-3524-e063-6294a90a3fd4", "dosage_form": "TABLET", "product_ndc": "61919-166", "generic_name": "BUSPIRONE HYDROCHLORIDE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUSPIRONE HYDROCHLORIDE", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202557", "marketing_category": "ANDA", "marketing_start_date": "20190726", "listing_expiration_date": "20271231"}