diclofenac potassium

Generic: diclofenac potassium

Labeler: leading pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler leading pharma, llc
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

diclofenac potassium 50 mg/1

Manufacturer
Leading Pharma, LLC

Identifiers & Regulatory

Product NDC 69315-506
Product ID 69315-506_9c24af27-0a21-4fb7-a8fb-55c92373b852
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA022165
Listing Expiration 2026-12-31
Marketing Start 2022-12-20

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] decreased prostaglandin production [pe] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69315506
Hyphenated Format 69315-506

Supplemental Identifiers

RxCUI
859063
UNII
L4D5UA6CB4

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 diclofenac potassium (source: ndc)
Generic Name diclofenac potassium (source: ndc)
Application Number NDA022165 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 9 PACKET in 1 CARTON (69315-506-09) / 1 POWDER, FOR SOLUTION in 1 PACKET
source: ndc

Packages (1)

69315-506-09 9 PACKET in 1 CARTON (69315-506-09) / 1 POWDER, FOR SOLUTION in 1 PACKET

Ingredients (1)

diclofenac potassium (50 mg/1)

Linked Drug Pages (1)

DICLOFENAC POTASSIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9c24af27-0a21-4fb7-a8fb-55c92373b852", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["859063"], "spl_set_id": ["9dd418b2-4b0e-498c-b453-f580c69ddc6d"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 PACKET in 1 CARTON (69315-506-09)  / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "69315-506-09", "marketing_start_date": "20221220"}], "brand_name": "DICLOFENAC POTASSIUM", "product_id": "69315-506_9c24af27-0a21-4fb7-a8fb-55c92373b852", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69315-506", "generic_name": "DICLOFENAC POTASSIUM", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DICLOFENAC POTASSIUM", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "NDA022165", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20221220", "listing_expiration_date": "20261231"}