buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 7.5 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-390
Product ID 59651-390_270d4008-311a-4f5c-905e-95f14bd9f700
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078246
Listing Expiration 2026-12-31
Marketing Start 2020-02-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651390
Hyphenated Format 59651-390

Supplemental Identifiers

RxCUI
866018 866083 866090 866094 866111
UPC
0359651392300
UNII
207LT9J9OC

Packaging Origin

Original Packager
true

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 ANDA078246 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59651-390-01)
  • 500 TABLET in 1 BOTTLE (59651-390-05)
source: ndc

Packages (2)

59651-390-01 100 TABLET in 1 BOTTLE (59651-390-01) 59651-390-05 500 TABLET in 1 BOTTLE (59651-390-05)

Ingredients (1)

buspirone hydrochloride (7.5 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": "270d4008-311a-4f5c-905e-95f14bd9f700", "openfda": {"upc": ["0359651392300"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["05c006d2-44b9-431f-bce2-aff09c043ecb"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-390-01)", "package_ndc": "59651-390-01", "marketing_start_date": "20200221"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (59651-390-05)", "package_ndc": "59651-390-05", "marketing_start_date": "20200221"}], "brand_name": "BUSPIRONE HYDROCHLORIDE", "product_id": "59651-390_270d4008-311a-4f5c-905e-95f14bd9f700", "dosage_form": "TABLET", "product_ndc": "59651-390", "generic_name": "BUSPIRONE HYDROCHLORIDE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUSPIRONE HYDROCHLORIDE", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078246", "marketing_category": "ANDA", "marketing_start_date": "20200221", "listing_expiration_date": "20261231"}