dichlorphenamide

Generic: dichlorphenamide

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

Drug Facts

Product Profile

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

dichlorphenamide 50 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-242
Product ID 16571-242_3ef66eca-f35a-46a8-bebe-b286dfbbb376
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218783
Listing Expiration 2026-12-31
Marketing Start 2025-11-18

Pharmacologic Class

Established (EPC)
carbonic anhydrase inhibitor [epc]
Mechanism of Action
carbonic anhydrase inhibitors [moa]
Chemical Structure
sulfonamides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16571242
Hyphenated Format 16571-242

Supplemental Identifiers

RxCUI
197594
UPC
0316571242016
UNII
VVJ6673MHY
NUI
N0000175517 N0000000235 M0020790

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 dichlorphenamide (source: ndc)
Generic Name dichlorphenamide (source: ndc)
Application Number ANDA218783 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (16571-242-01)
source: ndc

Packages (1)

16571-242-01 100 TABLET in 1 BOTTLE (16571-242-01)

Ingredients (1)

dichlorphenamide (50 mg/1)

Linked Drug Pages (1)

Dichlorphenamide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ef66eca-f35a-46a8-bebe-b286dfbbb376", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "upc": ["0316571242016"], "unii": ["VVJ6673MHY"], "rxcui": ["197594"], "spl_set_id": ["35b9c81a-5062-451d-8b0c-1b599113aa6c"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-242-01)", "package_ndc": "16571-242-01", "marketing_start_date": "20251118"}], "brand_name": "Dichlorphenamide", "product_id": "16571-242_3ef66eca-f35a-46a8-bebe-b286dfbbb376", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "16571-242", "generic_name": "Dichlorphenamide", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dichlorphenamide", "active_ingredients": [{"name": "DICHLORPHENAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA218783", "marketing_category": "ANDA", "marketing_start_date": "20251118", "listing_expiration_date": "20261231"}