buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

buspirone hydrochloride 10 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7121
Product ID 0904-7121_7e3f9aeb-2fcc-4f4d-921b-a4b96a932d19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204582
Listing Expiration 2026-12-31
Marketing Start 2012-06-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047121
Hyphenated Format 0904-7121

Supplemental Identifiers

RxCUI
866083 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 ANDA204582 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7121-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7121-61 100 BLISTER PACK in 1 CARTON (0904-7121-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

buspirone hydrochloride (10 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": "7e3f9aeb-2fcc-4f4d-921b-a4b96a932d19", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083", "866094"], "spl_set_id": ["8dc1ee33-e5aa-4462-8fb9-9bbdf5463488"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7121-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7121-61", "marketing_start_date": "20120629"}], "brand_name": "Buspirone Hydrochloride", "product_id": "0904-7121_7e3f9aeb-2fcc-4f4d-921b-a4b96a932d19", "dosage_form": "TABLET", "product_ndc": "0904-7121", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204582", "marketing_category": "ANDA", "marketing_start_date": "20120629", "listing_expiration_date": "20261231"}