diclofenac potassium

Generic: diclofenac potassium

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler aurobindo pharma limited
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

diclofenac potassium 25 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-353
Product ID 59651-353_69669299-a982-4891-9374-bfa88823c5f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213875
Listing Expiration 2026-12-31
Marketing Start 2022-03-14

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 59651353
Hyphenated Format 59651-353

Supplemental Identifiers

RxCUI
858342
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 ANDA213875 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (59651-353-01)
  • 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (59651-353-08)
source: ndc

Packages (2)

59651-353-01 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (59651-353-01) 59651-353-08 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (59651-353-08)

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": "69669299-a982-4891-9374-bfa88823c5f2", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["858342"], "spl_set_id": ["7efdbe23-503a-4f38-a0b6-c003033f0de7"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, LIQUID FILLED in 1 BOTTLE (59651-353-01)", "package_ndc": "59651-353-01", "marketing_start_date": "20220314"}, {"sample": false, "description": "120 CAPSULE, LIQUID FILLED in 1 BOTTLE (59651-353-08)", "package_ndc": "59651-353-08", "marketing_start_date": "20220314"}], "brand_name": "Diclofenac Potassium", "product_id": "59651-353_69669299-a982-4891-9374-bfa88823c5f2", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "59651-353", "generic_name": "Diclofenac Potassium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA213875", "marketing_category": "ANDA", "marketing_start_date": "20220314", "listing_expiration_date": "20261231"}