buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: accord healthcare inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler accord healthcare inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 7.5 mg/1

Manufacturer
Accord Healthcare Inc.

Identifiers & Regulatory

Product NDC 16729-201
Product ID 16729-201_4092e48b-b3d6-abf3-e063-6394a90afe61
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 16729201
Hyphenated Format 16729-201

Supplemental Identifiers

RxCUI
866018 866083 866090 866094 866111
UPC
0316729289016
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 ANDA202557 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (16729-201-01)
source: ndc

Packages (1)

16729-201-01 100 TABLET in 1 BOTTLE (16729-201-01)

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": "4092e48b-b3d6-abf3-e063-6394a90afe61", "openfda": {"upc": ["0316729289016"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["3da22999-f5fb-49fd-acde-c3006598e985"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16729-201-01)", "package_ndc": "16729-201-01", "marketing_start_date": "20161114"}], "brand_name": "Buspirone Hydrochloride", "product_id": "16729-201_4092e48b-b3d6-abf3-e063-6394a90afe61", "dosage_form": "TABLET", "product_ndc": "16729-201", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Accord Healthcare Inc.", "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"}