diclofenac potassium

Generic: diclofenac potassium

Labeler: carwin pharmaceutical associates, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler carwin pharmaceutical associates, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diclofenac potassium 25 mg/1

Manufacturer
Carwin Pharmaceutical Associates, LLC

Identifiers & Regulatory

Product NDC 15370-185
Product ID 15370-185_95ce3601-808d-47ed-9fe0-0f974068c075
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076561
Listing Expiration 2026-12-31
Marketing Start 2023-11-01

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 15370185
Hyphenated Format 15370-185

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 ANDA076561 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (15370-185-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (15370-185-60)
source: ndc

Packages (2)

15370-185-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (15370-185-30) 15370-185-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (15370-185-60)

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": "95ce3601-808d-47ed-9fe0-0f974068c075", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["857702"], "spl_set_id": ["bce95bb3-3097-4e7d-8d29-0870bb729212"], "manufacturer_name": ["Carwin Pharmaceutical Associates, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (15370-185-30)", "package_ndc": "15370-185-30", "marketing_start_date": "20231101"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (15370-185-60)", "package_ndc": "15370-185-60", "marketing_start_date": "20250408"}], "brand_name": "Diclofenac Potassium", "product_id": "15370-185_95ce3601-808d-47ed-9fe0-0f974068c075", "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": "15370-185", "generic_name": "DICLOFENAC POTASSIUM", "labeler_name": "Carwin Pharmaceutical Associates, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA076561", "marketing_category": "ANDA", "marketing_start_date": "20231101", "listing_expiration_date": "20261231"}