buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-139
Product ID 72789-139_4b96ead2-cbe0-fb3c-e063-6294a90ad561
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075388
Listing Expiration 2027-12-31
Marketing Start 2020-07-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789139
Hyphenated Format 72789-139

Supplemental Identifiers

RxCUI
866018 866083 866090 866094
UPC
0372789141015 0372789140018 0372789139012 0372789142609
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 ANDA075388 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-139-01)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-139-60)
source: ndc

Packages (2)

72789-139-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-139-01) 72789-139-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-139-60)

Ingredients (1)

buspirone hydrochloride (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": "4b96ead2-cbe0-fb3c-e063-6294a90ad561", "openfda": {"upc": ["0372789141015", "0372789140018", "0372789139012", "0372789142609"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["476f4f55-c6c1-4f39-950e-59236f499577"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-139-01)", "package_ndc": "72789-139-01", "marketing_start_date": "20201106"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-139-60)", "package_ndc": "72789-139-60", "marketing_start_date": "20260224"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72789-139_4b96ead2-cbe0-fb3c-e063-6294a90ad561", "dosage_form": "TABLET", "product_ndc": "72789-139", "generic_name": "buspirone hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20271231"}