diclofenac sodium

Generic: diclofenac sodium

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac sodium
Generic Name diclofenac sodium
Labeler proficient rx lp
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

diclofenac sodium 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-522
Product ID 63187-522_f202c634-42a1-4983-8aa6-05d62ddd0892
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074514
Listing Expiration 2026-12-31
Marketing Start 1996-03-26

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 63187522
Hyphenated Format 63187-522

Supplemental Identifiers

RxCUI
855906
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 ANDA074514 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-522-30)
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-522-60)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-522-90)
source: ndc

Packages (3)

63187-522-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-522-30) 63187-522-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-522-60) 63187-522-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-522-90)

Ingredients (1)

diclofenac sodium (50 mg/1)

Linked Drug Pages (1)

Diclofenac Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f202c634-42a1-4983-8aa6-05d62ddd0892", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["f5b4e308-c156-4865-95ee-1a8e267535ba"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-522-30)", "package_ndc": "63187-522-30", "marketing_start_date": "20150201"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-522-60)", "package_ndc": "63187-522-60", "marketing_start_date": "20150201"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-522-90)", "package_ndc": "63187-522-90", "marketing_start_date": "20150201"}], "brand_name": "Diclofenac Sodium", "product_id": "63187-522_f202c634-42a1-4983-8aa6-05d62ddd0892", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63187-522", "generic_name": "Diclofenac Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA074514", "marketing_category": "ANDA", "marketing_start_date": "19960326", "listing_expiration_date": "20261231"}