buspirone hydrochloride

Generic: buspirone hydrochloride

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

Drug Facts

Product Profile

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

buspirone hydrochloride 15 mg/1

Manufacturer
Strides Pharma Science Limited

Identifiers & Regulatory

Product NDC 64380-743
Product ID 64380-743_8b51cc64-78c9-4457-a523-161bc2049bdf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202330
Listing Expiration 2026-12-31
Marketing Start 2015-06-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64380743
Hyphenated Format 64380-743

Supplemental Identifiers

RxCUI
866018 866083 866090 866094 866111
UPC
0364380744030 0364380741077 0364380743064 0364380743187 0364380742081 0364380741084 0364380741060 0364380787068 0364380787075 0364380743033 0364380742074 0364380742067
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 ANDA202330 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (64380-743-03)
  • 100 TABLET in 1 BOTTLE (64380-743-06)
  • 180 TABLET in 1 BOTTLE (64380-743-18)
source: ndc

Packages (3)

64380-743-03 60 TABLET in 1 BOTTLE (64380-743-03) 64380-743-06 100 TABLET in 1 BOTTLE (64380-743-06) 64380-743-18 180 TABLET in 1 BOTTLE (64380-743-18)

Ingredients (1)

buspirone hydrochloride (15 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": "8b51cc64-78c9-4457-a523-161bc2049bdf", "openfda": {"upc": ["0364380744030", "0364380741077", "0364380743064", "0364380743187", "0364380742081", "0364380741084", "0364380741060", "0364380787068", "0364380787075", "0364380743033", "0364380742074", "0364380742067"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["cff9f09a-1ea2-4968-b57b-e62bebaae238"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (64380-743-03)", "package_ndc": "64380-743-03", "marketing_start_date": "20150630"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (64380-743-06)", "package_ndc": "64380-743-06", "marketing_start_date": "20150630"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (64380-743-18)", "package_ndc": "64380-743-18", "marketing_start_date": "20150630"}], "brand_name": "Buspirone Hydrochloride", "product_id": "64380-743_8b51cc64-78c9-4457-a523-161bc2049bdf", "dosage_form": "TABLET", "product_ndc": "64380-743", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA202330", "marketing_category": "ANDA", "marketing_start_date": "20150630", "listing_expiration_date": "20261231"}