arthritis pain reliever

Generic: diclofenac sodium

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arthritis pain reliever
Generic Name diclofenac sodium
Labeler p & l development, llc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

diclofenac sodium 10 mg/g

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-012
Product ID 59726-012_4a226f9f-95f7-47bf-8f9e-741ecea07fe1
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA208077
Listing Expiration 2026-12-31
Marketing Start 2021-06-25

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 59726012
Hyphenated Format 59726-012

Supplemental Identifiers

RxCUI
855633
UPC
0359726012355
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 arthritis pain reliever (source: ndc)
Generic Name diclofenac sodium (source: ndc)
Application Number ANDA208077 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (59726-012-50) / 50 g in 1 TUBE
  • 1 TUBE in 1 CARTON (59726-012-53) / 100 g in 1 TUBE
source: ndc

Packages (2)

Ingredients (1)

diclofenac sodium (10 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4a226f9f-95f7-47bf-8f9e-741ecea07fe1", "openfda": {"upc": ["0359726012355"], "unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["2596645a-b736-4d3c-82a0-00713f1b6fbd"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (59726-012-50)  / 50 g in 1 TUBE", "package_ndc": "59726-012-50", "marketing_start_date": "20210625"}, {"sample": false, "description": "1 TUBE in 1 CARTON (59726-012-53)  / 100 g in 1 TUBE", "package_ndc": "59726-012-53", "marketing_start_date": "20210625"}], "brand_name": "Arthritis Pain Reliever", "product_id": "59726-012_4a226f9f-95f7-47bf-8f9e-741ecea07fe1", "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": "59726-012", "generic_name": "Diclofenac sodium", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arthritis Pain Reliever", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA208077", "marketing_category": "ANDA", "marketing_start_date": "20210625", "listing_expiration_date": "20261231"}