diclofenac sodium

Generic: diclofenac sodium

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac sodium
Generic Name diclofenac sodium
Labeler sun pharmaceutical industries, inc.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

diclofenac sodium 30 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1363
Product ID 51672-1363_38ef9dc7-662f-056c-e063-6394a90a47e2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206298
Listing Expiration 2026-12-31
Marketing Start 2016-04-28

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 516721363
Hyphenated Format 51672-1363

Supplemental Identifiers

RxCUI
855642
UNII
QTG126297Q

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 sodium (source: ndc)
Generic Name diclofenac sodium (source: ndc)
Application Number ANDA206298 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-1363-3) / 50 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1363-7) / 100 g in 1 TUBE
source: ndc

Packages (2)

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": "38ef9dc7-662f-056c-e063-6394a90a47e2", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["aa1e1ed3-0444-4bf5-a0ee-5d21a7fca391"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1363-3)  / 50 g in 1 TUBE", "package_ndc": "51672-1363-3", "marketing_start_date": "20160428"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1363-7)  / 100 g in 1 TUBE", "package_ndc": "51672-1363-7", "marketing_start_date": "20160428"}], "brand_name": "Diclofenac sodium", "product_id": "51672-1363_38ef9dc7-662f-056c-e063-6394a90a47e2", "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": "51672-1363", "generic_name": "diclofenac sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "30 mg/g"}], "application_number": "ANDA206298", "marketing_category": "ANDA", "marketing_start_date": "20160428", "listing_expiration_date": "20261231"}