buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 10 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3336
Product ID 68071-3336_1cd71696-d959-be3e-e063-6394a90a28c8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202557
Listing Expiration 2026-12-31
Marketing Start 2016-12-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713336
Hyphenated Format 68071-3336

Supplemental Identifiers

RxCUI
866083
UPC
0368071333633
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 ANDA202557 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-3336-3)
  • 60 TABLET in 1 BOTTLE (68071-3336-6)
  • 90 TABLET in 1 BOTTLE (68071-3336-9)
source: ndc

Packages (3)

68071-3336-3 30 TABLET in 1 BOTTLE (68071-3336-3) 68071-3336-6 60 TABLET in 1 BOTTLE (68071-3336-6) 68071-3336-9 90 TABLET in 1 BOTTLE (68071-3336-9)

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": "1cd71696-d959-be3e-e063-6394a90a28c8", "openfda": {"upc": ["0368071333633"], "unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["540e9b7e-09ff-2cca-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3336-3)", "package_ndc": "68071-3336-3", "marketing_start_date": "20170711"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3336-6)", "package_ndc": "68071-3336-6", "marketing_start_date": "20170711"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3336-9)", "package_ndc": "68071-3336-9", "marketing_start_date": "20170711"}], "brand_name": "Buspirone Hydrochloride", "product_id": "68071-3336_1cd71696-d959-be3e-e063-6394a90a28c8", "dosage_form": "TABLET", "product_ndc": "68071-3336", "generic_name": "Buspirone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202557", "marketing_category": "ANDA", "marketing_start_date": "20161215", "listing_expiration_date": "20261231"}