diclofenac sodium

Generic: diclofenac sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac sodium
Generic Name diclofenac sodium
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diclofenac sodium 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4172
Product ID 50090-4172_9c9c3f13-4e0f-4f4a-8065-6bd89a25ff96
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075492
Listing Expiration 2026-12-31
Marketing Start 2000-02-28

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 500904172
Hyphenated Format 50090-4172

Supplemental Identifiers

RxCUI
855657
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 ANDA075492 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4172-1)
source: ndc

Packages (1)

50090-4172-1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4172-1)

Ingredients (1)

diclofenac sodium (100 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": "9c9c3f13-4e0f-4f4a-8065-6bd89a25ff96", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["d9698809-4887-4514-aa28-0066355ef908"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4172-1)", "package_ndc": "50090-4172-1", "marketing_start_date": "20190307"}], "brand_name": "Diclofenac Sodium", "product_id": "50090-4172_9c9c3f13-4e0f-4f4a-8065-6bd89a25ff96", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-4172", "generic_name": "Diclofenac Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA075492", "marketing_category": "ANDA", "marketing_start_date": "20000228", "listing_expiration_date": "20261231"}