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 15 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-332
Product ID 72789-332_401ffb0a-e4c9-09e1-e063-6294a90ade8b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075388
Listing Expiration 2026-12-31
Marketing Start 2020-07-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789332
Hyphenated Format 72789-332

Supplemental Identifiers

RxCUI
866018
UPC
0372789332604
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
  • 15 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-332-60)
source: ndc

Packages (1)

72789-332-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-332-60)

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": "401ffb0a-e4c9-09e1-e063-6294a90ade8b", "openfda": {"upc": ["0372789332604"], "unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["270398a0-21b8-407b-af76-4aeef90f72be"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-332-60)", "package_ndc": "72789-332-60", "marketing_start_date": "20230728"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72789-332_401ffb0a-e4c9-09e1-e063-6294a90ade8b", "dosage_form": "TABLET", "product_ndc": "72789-332", "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": "15 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20261231"}