buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 30 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4068
Product ID 70518-4068_3fa2e69e-0c7d-9409-e063-6394a90a7ccc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210907
Listing Expiration 2026-12-31
Marketing Start 2024-05-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184068
Hyphenated Format 70518-4068

Supplemental Identifiers

RxCUI
866090
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 ANDA210907 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-4068-0)
source: ndc

Packages (1)

70518-4068-0 30 TABLET in 1 BLISTER PACK (70518-4068-0)

Ingredients (1)

buspirone hydrochloride (30 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": "3fa2e69e-0c7d-9409-e063-6394a90a7ccc", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866090"], "spl_set_id": ["ed2b56fe-e02f-46bc-808a-352f9bbb5b57"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4068-0)", "package_ndc": "70518-4068-0", "marketing_start_date": "20240505"}], "brand_name": "Buspirone Hydrochloride", "product_id": "70518-4068_3fa2e69e-0c7d-9409-e063-6394a90a7ccc", "dosage_form": "TABLET", "product_ndc": "70518-4068", "generic_name": "Buspirone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20240505", "listing_expiration_date": "20261231"}