diclofenac potassium

Generic: diclofenac potassium

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diclofenac potassium 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-848
Product ID 43063-848_2fc3b270-b101-5a08-e063-6394a90a7fd2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075219
Listing Expiration 2026-12-31
Marketing Start 1998-08-11

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 43063848
Hyphenated Format 43063-848

Supplemental Identifiers

RxCUI
855942
UPC
0343063848210
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 ANDA075219 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-21)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-30)
source: ndc

Packages (2)

43063-848-21 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-21) 43063-848-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-30)

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": "2fc3b270-b101-5a08-e063-6394a90a7fd2", "openfda": {"upc": ["0343063848210"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["08e41a9d-644c-4ac6-aba3-38d7c3f36d36"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-21)", "package_ndc": "43063-848-21", "marketing_start_date": "20180412"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-30)", "package_ndc": "43063-848-30", "marketing_start_date": "20180412"}], "brand_name": "Diclofenac Potassium", "product_id": "43063-848_2fc3b270-b101-5a08-e063-6394a90a7fd2", "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": "43063-848", "generic_name": "Diclofenac Potassium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA075219", "marketing_category": "ANDA", "marketing_start_date": "19980811", "listing_expiration_date": "20261231"}