probenecid

Generic: probenecid

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name probenecid
Generic Name probenecid
Labeler lannett company, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

probenecid 500 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-1367
Product ID 0527-1367_8679dae4-b649-458d-962b-2afb0f491d2a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080966
Listing Expiration 2026-12-31
Marketing Start 1976-07-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05271367
Hyphenated Format 0527-1367

Supplemental Identifiers

RxCUI
198152
UPC
0305271367013
UNII
PO572Z7917

Packaging Origin

Original Packager
true

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 probenecid (source: ndc)
Generic Name probenecid (source: ndc)
Application Number ANDA080966 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0527-1367-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (0527-1367-10)
source: ndc

Packages (2)

0527-1367-01 100 TABLET, FILM COATED in 1 BOTTLE (0527-1367-01) 0527-1367-10 1000 TABLET, FILM COATED in 1 BOTTLE (0527-1367-10)

Ingredients (1)

probenecid (500 mg/1)

Linked Drug Pages (1)

Probenecid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8679dae4-b649-458d-962b-2afb0f491d2a", "openfda": {"upc": ["0305271367013"], "unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["ab497fd8-00c3-4364-b003-b39d21fbdf38"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0527-1367-01)", "package_ndc": "0527-1367-01", "marketing_start_date": "19760729"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0527-1367-10)", "package_ndc": "0527-1367-10", "marketing_start_date": "19760729"}], "brand_name": "Probenecid", "product_id": "0527-1367_8679dae4-b649-458d-962b-2afb0f491d2a", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0527-1367", "generic_name": "Probenecid", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Probenecid", "active_ingredients": [{"name": "PROBENECID", "strength": "500 mg/1"}], "application_number": "ANDA080966", "marketing_category": "ANDA", "marketing_start_date": "19760729", "listing_expiration_date": "20261231"}