diclofenac sodium

Generic: diclofenac sodium

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac sodium
Generic Name diclofenac sodium
Labeler asclemed usa, inc.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

diclofenac sodium 30 mg/g

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-025
Product ID 76420-025_a843b00f-4da3-1901-e053-2a95a90affae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200936
Listing Expiration 2026-12-31
Marketing Start 2013-11-21

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 76420025
Hyphenated Format 76420-025

Supplemental Identifiers

RxCUI
855642
UNII
QTG126297Q

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 sodium (source: ndc)
Generic Name diclofenac sodium (source: ndc)
Application Number ANDA200936 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/g
source: ndc
Packaging
  • 100 g in 1 TUBE (76420-025-01)
source: ndc

Packages (1)

Ingredients (1)

diclofenac sodium (30 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "a843b00f-4da3-1901-e053-2a95a90affae", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["1e39f8d4-56a2-4d29-a971-495574e8d4a7"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 g in 1 TUBE (76420-025-01)", "package_ndc": "76420-025-01", "marketing_start_date": "20200617"}], "brand_name": "Diclofenac Sodium", "product_id": "76420-025_a843b00f-4da3-1901-e053-2a95a90affae", "dosage_form": "GEL", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "76420-025", "generic_name": "Diclofenac Sodium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "30 mg/g"}], "application_number": "ANDA200936", "marketing_category": "ANDA", "marketing_start_date": "20131121", "listing_expiration_date": "20261231"}