buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

buspirone hydrochloride 15 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-135
Product ID 50268-135_47e23c78-47b4-7a49-e063-6394a90a4e81
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078888
Listing Expiration 2027-12-31
Marketing Start 2020-10-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268135
Hyphenated Format 50268-135

Supplemental Identifiers

RxCUI
866018
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 ANDA078888 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-135-15) / 1 TABLET in 1 BLISTER PACK (50268-135-11)
source: ndc

Packages (1)

50268-135-15 50 BLISTER PACK in 1 BOX (50268-135-15) / 1 TABLET in 1 BLISTER PACK (50268-135-11)

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": "47e23c78-47b4-7a49-e063-6394a90a4e81", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["b230197c-3d50-7874-e053-2a95a90af50f"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-135-15)  / 1 TABLET in 1 BLISTER PACK (50268-135-11)", "package_ndc": "50268-135-15", "marketing_start_date": "20201021"}], "brand_name": "Buspirone hydrochloride", "product_id": "50268-135_47e23c78-47b4-7a49-e063-6394a90a4e81", "dosage_form": "TABLET", "product_ndc": "50268-135", "generic_name": "Buspirone hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20201021", "listing_expiration_date": "20271231"}