probenecid

Generic: probenecid

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name probenecid
Generic Name probenecid
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

probenecid 500 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-831
Product ID 16571-831_5b9e2e37-77b7-464f-9bc8-ff678643d773
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217020
Listing Expiration 2027-12-31
Marketing Start 2023-11-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16571831
Hyphenated Format 16571-831

Supplemental Identifiers

RxCUI
198152
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 ANDA217020 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 CONTAINER (16571-831-01)
  • 1000 TABLET in 1 CONTAINER (16571-831-10)
source: ndc

Packages (2)

Ingredients (1)

probenecid (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5b9e2e37-77b7-464f-9bc8-ff678643d773", "openfda": {"unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["f2375d90-4132-4fb6-aee7-c4f9d11e98d5"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CONTAINER (16571-831-01)", "package_ndc": "16571-831-01", "marketing_start_date": "20231120"}, {"sample": false, "description": "1000 TABLET in 1 CONTAINER (16571-831-10)", "package_ndc": "16571-831-10", "marketing_start_date": "20231120"}], "brand_name": "Probenecid", "product_id": "16571-831_5b9e2e37-77b7-464f-9bc8-ff678643d773", "dosage_form": "TABLET", "product_ndc": "16571-831", "generic_name": "Probenecid", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Probenecid", "active_ingredients": [{"name": "PROBENECID", "strength": "500 mg/1"}], "application_number": "ANDA217020", "marketing_category": "ANDA", "marketing_start_date": "20231120", "listing_expiration_date": "20271231"}