diclofenac potassium

Generic: diclofenac potassium

Labeler: trifluent pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler trifluent pharma llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diclofenac potassium 25 mg/1

Manufacturer
Trifluent Pharma LLC

Identifiers & Regulatory

Product NDC 73352-086
Product ID 73352-086_e1409a25-9dd7-4c50-ae45-7dbaee133125
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075229
Listing Expiration 2026-12-31
Marketing Start 2023-02-17

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 73352086
Hyphenated Format 73352-086

Supplemental Identifiers

RxCUI
857702
UNII
L4D5UA6CB4

Packaging Origin

Original Packager
true

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
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (73352-086-30)
  • 60 TABLET, COATED in 1 BOTTLE (73352-086-60)
source: ndc

Packages (2)

73352-086-30 30 TABLET, COATED in 1 BOTTLE (73352-086-30) 73352-086-60 60 TABLET, COATED in 1 BOTTLE (73352-086-60)

Ingredients (1)

diclofenac potassium (25 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": "e1409a25-9dd7-4c50-ae45-7dbaee133125", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["857702"], "spl_set_id": ["8fdb1036-c0d8-4288-ac37-6512b05672ef"], "manufacturer_name": ["Trifluent Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (73352-086-30)", "package_ndc": "73352-086-30", "marketing_start_date": "20230217"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (73352-086-60)", "package_ndc": "73352-086-60", "marketing_start_date": "20230925"}], "brand_name": "Diclofenac Potassium", "product_id": "73352-086_e1409a25-9dd7-4c50-ae45-7dbaee133125", "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": "73352-086", "generic_name": "diclofenac potassium", "labeler_name": "Trifluent Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA075229", "marketing_category": "ANDA", "marketing_start_date": "20230217", "listing_expiration_date": "20261231"}