diclofenac potassium

Generic: diclofenac potassium

Labeler: advagen pharma ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

diclofenac potassium 50 mg/1

Manufacturer
Advagen Pharma Ltd

Identifiers & Regulatory

Product NDC 72888-073
Product ID 72888-073_473c6621-0a69-12fd-e063-6294a90a1fb8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075229
Listing Expiration 2026-12-31
Marketing Start 2020-12-19

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 72888073
Hyphenated Format 72888-073

Supplemental Identifiers

RxCUI
855942 857702
UPC
0372888073309 0372888086002 0372888073002 0372888086019 0372888073019 0372888086309 0372888073057
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
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET, COATED in 1 BOTTLE (72888-073-00)
  • 100 TABLET, COATED in 1 BOTTLE (72888-073-01)
  • 500 TABLET, COATED in 1 BOTTLE (72888-073-05)
  • 30 TABLET, COATED in 1 BOTTLE (72888-073-30)
source: ndc

Packages (4)

72888-073-00 1000 TABLET, COATED in 1 BOTTLE (72888-073-00) 72888-073-01 100 TABLET, COATED in 1 BOTTLE (72888-073-01) 72888-073-05 500 TABLET, COATED in 1 BOTTLE (72888-073-05) 72888-073-30 30 TABLET, COATED in 1 BOTTLE (72888-073-30)

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": "473c6621-0a69-12fd-e063-6294a90a1fb8", "openfda": {"upc": ["0372888073309", "0372888086002", "0372888073002", "0372888086019", "0372888073019", "0372888086309", "0372888073057"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942", "857702"], "spl_set_id": ["82218d5c-1625-471a-aabe-f43338e5176b"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (72888-073-00)", "package_ndc": "72888-073-00", "marketing_start_date": "20201219"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (72888-073-01)", "package_ndc": "72888-073-01", "marketing_start_date": "20201219"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (72888-073-05)", "package_ndc": "72888-073-05", "marketing_start_date": "20220203"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72888-073-30)", "package_ndc": "72888-073-30", "marketing_start_date": "20201219"}], "brand_name": "Diclofenac Potassium", "product_id": "72888-073_473c6621-0a69-12fd-e063-6294a90a1fb8", "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": "72888-073", "generic_name": "diclofenac potassium", "labeler_name": "Advagen Pharma Ltd", "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": "20201219", "listing_expiration_date": "20261231"}