buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 7.5 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-801
Product ID 60687-801_1a4e0770-e1ad-f44a-e063-6294a90a8257
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078888
Listing Expiration 2026-12-31
Marketing Start 2024-02-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687801
Hyphenated Format 60687-801

Supplemental Identifiers

RxCUI
866018 866083 866111
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 ANDA078888 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-801-21) / 1 TABLET in 1 BLISTER PACK (60687-801-11)
source: ndc

Packages (1)

Ingredients (1)

buspirone hydrochloride (7.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a4e0770-e1ad-f44a-e063-6294a90a8257", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866111"], "spl_set_id": ["e80d83a6-7c2a-478e-bdf1-c481824fc301"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-801-21)  / 1 TABLET in 1 BLISTER PACK (60687-801-11)", "package_ndc": "60687-801-21", "marketing_start_date": "20240221"}], "brand_name": "Buspirone hydrochloride", "product_id": "60687-801_1a4e0770-e1ad-f44a-e063-6294a90a8257", "dosage_form": "TABLET", "product_ndc": "60687-801", "generic_name": "Buspirone hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20240221", "listing_expiration_date": "20261231"}