diclofenac potassium

Generic: diclofenac potassium

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diclofenac potassium 50 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2625
Product ID 68071-2625_2baf0832-b4e3-f7fc-e063-6394a90a52da
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075229
Listing Expiration 2026-12-31
Marketing Start 2021-03-20

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 680712625
Hyphenated Format 68071-2625

Supplemental Identifiers

RxCUI
855942
UPC
0368071262599
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 (68071-2625-3)
  • 60 TABLET, COATED in 1 BOTTLE (68071-2625-6)
  • 9 TABLET, COATED in 1 BOTTLE (68071-2625-9)
source: ndc

Packages (3)

68071-2625-3 30 TABLET, COATED in 1 BOTTLE (68071-2625-3) 68071-2625-6 60 TABLET, COATED in 1 BOTTLE (68071-2625-6) 68071-2625-9 9 TABLET, COATED in 1 BOTTLE (68071-2625-9)

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": "2baf0832-b4e3-f7fc-e063-6394a90a52da", "openfda": {"upc": ["0368071262599"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["d61cbb27-737d-948c-e053-2a95a90adaca"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68071-2625-3)", "package_ndc": "68071-2625-3", "marketing_start_date": "20220121"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68071-2625-6)", "package_ndc": "68071-2625-6", "marketing_start_date": "20250114"}, {"sample": false, "description": "9 TABLET, COATED in 1 BOTTLE (68071-2625-9)", "package_ndc": "68071-2625-9", "marketing_start_date": "20220121"}], "brand_name": "Diclofenac Potassium", "product_id": "68071-2625_2baf0832-b4e3-f7fc-e063-6394a90a52da", "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": "68071-2625", "generic_name": "diclofenac potassium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20210320", "listing_expiration_date": "20261231"}