diclofenac potassium

Generic: diclofenac potassium tablets

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 tablets
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diclofenac potassium 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6768
Product ID 50090-6768_fe1e72df-f70a-4e79-8ebf-10f3a9983961
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215750
Listing Expiration 2026-12-31
Marketing Start 2022-05-12

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 500906768
Hyphenated Format 50090-6768

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 tablets (source: ndc)
Application Number ANDA215750 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-6768-0)
  • 21 TABLET, FILM COATED in 1 BOTTLE (50090-6768-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-6768-4)
source: ndc

Packages (3)

50090-6768-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-6768-0) 50090-6768-1 21 TABLET, FILM COATED in 1 BOTTLE (50090-6768-1) 50090-6768-4 90 TABLET, FILM COATED in 1 BOTTLE (50090-6768-4)

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": "fe1e72df-f70a-4e79-8ebf-10f3a9983961", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["5d37fc5a-7a2f-432e-b4e9-e00c246ce33c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6768-0)", "package_ndc": "50090-6768-0", "marketing_start_date": "20231023"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (50090-6768-1)", "package_ndc": "50090-6768-1", "marketing_start_date": "20231023"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6768-4)", "package_ndc": "50090-6768-4", "marketing_start_date": "20231023"}], "brand_name": "Diclofenac Potassium", "product_id": "50090-6768_fe1e72df-f70a-4e79-8ebf-10f3a9983961", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-6768", "generic_name": "Diclofenac Potassium Tablets", "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": "ANDA215750", "marketing_category": "ANDA", "marketing_start_date": "20220512", "listing_expiration_date": "20261231"}