buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 7.5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5614
Product ID 50090-5614_97b4a6a7-d4fa-499e-aad4-0ed13cf8e4e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202557
Listing Expiration 2026-12-31
Marketing Start 2016-11-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905614
Hyphenated Format 50090-5614

Supplemental Identifiers

RxCUI
866111
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
  • 7.5 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (50090-5614-0)
source: ndc

Packages (1)

50090-5614-0 60 TABLET in 1 BOTTLE (50090-5614-0)

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": "97b4a6a7-d4fa-499e-aad4-0ed13cf8e4e8", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["4ae45cb1-8612-4006-b12c-2440160132ac"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-5614-0)", "package_ndc": "50090-5614-0", "marketing_start_date": "20210818"}], "brand_name": "Buspirone Hydrochloride", "product_id": "50090-5614_97b4a6a7-d4fa-499e-aad4-0ed13cf8e4e8", "dosage_form": "TABLET", "product_ndc": "50090-5614", "generic_name": "Buspirone Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA202557", "marketing_category": "ANDA", "marketing_start_date": "20161114", "listing_expiration_date": "20261231"}