buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 30 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-247
Product ID 29300-247_ef78a61a-865b-447a-9324-3044e41db506
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210907
Listing Expiration 2026-12-31
Marketing Start 2019-11-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 29300247
Hyphenated Format 29300-247

Supplemental Identifiers

RxCUI
866018 866083 866090 866094
UPC
0329300246018 0329300245011 0329300247015
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 ANDA210907 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (29300-247-01)
  • 500 TABLET in 1 BOTTLE, PLASTIC (29300-247-05)
  • 60 TABLET in 1 BOTTLE, PLASTIC (29300-247-16)
source: ndc

Packages (3)

29300-247-01 100 TABLET in 1 BOTTLE, PLASTIC (29300-247-01) 29300-247-05 500 TABLET in 1 BOTTLE, PLASTIC (29300-247-05) 29300-247-16 60 TABLET in 1 BOTTLE, PLASTIC (29300-247-16)

Ingredients (1)

buspirone hydrochloride (30 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": "ef78a61a-865b-447a-9324-3044e41db506", "openfda": {"upc": ["0329300246018", "0329300245011", "0329300247015"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["a6bdf140-075e-445e-a62d-633a4b97f3a8"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (29300-247-01)", "package_ndc": "29300-247-01", "marketing_start_date": "20191120"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (29300-247-05)", "package_ndc": "29300-247-05", "marketing_start_date": "20191120"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (29300-247-16)", "package_ndc": "29300-247-16", "marketing_start_date": "20191120"}], "brand_name": "Buspirone Hydrochloride", "product_id": "29300-247_ef78a61a-865b-447a-9324-3044e41db506", "dosage_form": "TABLET", "product_ndc": "29300-247", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20191114", "listing_expiration_date": "20261231"}