buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler direct rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 10 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-200
Product ID 72189-200_4c498a8f-f65a-5df5-e063-6394a90ae0fd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202330
Listing Expiration 2027-12-31
Marketing Start 2021-04-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189200
Hyphenated Format 72189-200

Supplemental Identifiers

RxCUI
866083
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 ANDA202330 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 180 TABLET in 1 BOTTLE (72189-200-82)
source: ndc

Packages (1)

72189-200-82 180 TABLET in 1 BOTTLE (72189-200-82)

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": "4c498a8f-f65a-5df5-e063-6394a90ae0fd", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["bae98d45-e192-56e3-e053-2a95a90aadc3"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (72189-200-82)", "package_ndc": "72189-200-82", "marketing_start_date": "20210412"}], "brand_name": "BUSPIRONE HYDROCHLORIDE", "product_id": "72189-200_4c498a8f-f65a-5df5-e063-6394a90ae0fd", "dosage_form": "TABLET", "product_ndc": "72189-200", "generic_name": "BUSPIRONE HYDROCHLORIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUSPIRONE HYDROCHLORIDE", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202330", "marketing_category": "ANDA", "marketing_start_date": "20210412", "listing_expiration_date": "20271231"}