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 10 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-181
Product ID 72789-181_4019e519-dc9e-1fc4-e063-6294a90a8865
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 72789181
Hyphenated Format 72789-181

Supplemental Identifiers

RxCUI
866083
UPC
0372789181905
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
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-181-90)
source: ndc

Packages (1)

72789-181-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-181-90)

Ingredients (1)

buspirone hydrochloride (10 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": "4019e519-dc9e-1fc4-e063-6294a90a8865", "openfda": {"upc": ["0372789181905"], "unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["b217f341-7d51-475d-887f-f16786164c7b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-181-90)", "package_ndc": "72789-181-90", "marketing_start_date": "20210413"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72789-181_4019e519-dc9e-1fc4-e063-6294a90a8865", "dosage_form": "TABLET", "product_ndc": "72789-181", "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": "10 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20261231"}