diclofenac potassium

Generic: diclofenac potassium

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

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler a-s medication solutions
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diclofenac potassium 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5893
Product ID 50090-5893_b6546725-2742-4aef-a3cf-0c53aeaea638
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075229
Listing Expiration 2026-12-31
Marketing Start 2020-12-19

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 500905893
Hyphenated Format 50090-5893

Supplemental Identifiers

RxCUI
855942
UNII
L4D5UA6CB4

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 potassium (source: ndc)
Generic Name diclofenac potassium (source: ndc)
Application Number ANDA075229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (50090-5893-0)
  • 21 TABLET, COATED in 1 BOTTLE (50090-5893-1)
  • 45 TABLET, COATED in 1 BOTTLE (50090-5893-3)
  • 90 TABLET, COATED in 1 BOTTLE (50090-5893-4)
source: ndc

Packages (4)

50090-5893-0 30 TABLET, COATED in 1 BOTTLE (50090-5893-0) 50090-5893-1 21 TABLET, COATED in 1 BOTTLE (50090-5893-1) 50090-5893-3 45 TABLET, COATED in 1 BOTTLE (50090-5893-3) 50090-5893-4 90 TABLET, COATED in 1 BOTTLE (50090-5893-4)

Ingredients (1)

diclofenac potassium (50 mg/1)

Linked Drug Pages (1)

Diclofenac Potassium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b6546725-2742-4aef-a3cf-0c53aeaea638", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["112e7c94-23c8-451e-ae71-eb89a6eb2cb2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (50090-5893-0)", "package_ndc": "50090-5893-0", "marketing_start_date": "20220112"}, {"sample": false, "description": "21 TABLET, COATED in 1 BOTTLE (50090-5893-1)", "package_ndc": "50090-5893-1", "marketing_start_date": "20220116"}, {"sample": false, "description": "45 TABLET, COATED in 1 BOTTLE (50090-5893-3)", "package_ndc": "50090-5893-3", "marketing_start_date": "20220116"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-5893-4)", "package_ndc": "50090-5893-4", "marketing_start_date": "20220116"}], "brand_name": "Diclofenac Potassium", "product_id": "50090-5893_b6546725-2742-4aef-a3cf-0c53aeaea638", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-5893", "generic_name": "diclofenac potassium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA075229", "marketing_category": "ANDA", "marketing_start_date": "20201219", "listing_expiration_date": "20261231"}