diclofenac potassium

Generic: diclofenac potassium

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler bryant ranch prepack
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diclofenac potassium 50 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2052
Product ID 71335-2052_5c0968a7-d80a-4a70-8e03-6a88d72c2545
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 713352052
Hyphenated Format 71335-2052

Supplemental Identifiers

RxCUI
855942
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 ANDA075229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 20 TABLET, COATED in 1 BOTTLE (71335-2052-1)
  • 90 TABLET, COATED in 1 BOTTLE (71335-2052-2)
  • 30 TABLET, COATED in 1 BOTTLE (71335-2052-3)
  • 60 TABLET, COATED in 1 BOTTLE (71335-2052-4)
  • 45 TABLET, COATED in 1 BOTTLE (71335-2052-5)
  • 58 TABLET, COATED in 1 BOTTLE (71335-2052-6)
  • 18 TABLET, COATED in 1 BOTTLE (71335-2052-7)
  • 120 TABLET, COATED in 1 BOTTLE (71335-2052-8)
source: ndc

Packages (8)

71335-2052-1 20 TABLET, COATED in 1 BOTTLE (71335-2052-1) 71335-2052-2 90 TABLET, COATED in 1 BOTTLE (71335-2052-2) 71335-2052-3 30 TABLET, COATED in 1 BOTTLE (71335-2052-3) 71335-2052-4 60 TABLET, COATED in 1 BOTTLE (71335-2052-4) 71335-2052-5 45 TABLET, COATED in 1 BOTTLE (71335-2052-5) 71335-2052-6 58 TABLET, COATED in 1 BOTTLE (71335-2052-6) 71335-2052-7 18 TABLET, COATED in 1 BOTTLE (71335-2052-7) 71335-2052-8 120 TABLET, COATED in 1 BOTTLE (71335-2052-8)

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": "5c0968a7-d80a-4a70-8e03-6a88d72c2545", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["86461915-9bc1-43d4-8d92-6eef3e56bd90"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (71335-2052-1)", "package_ndc": "71335-2052-1", "marketing_start_date": "20220318"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-2052-2)", "package_ndc": "71335-2052-2", "marketing_start_date": "20220318"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71335-2052-3)", "package_ndc": "71335-2052-3", "marketing_start_date": "20220316"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (71335-2052-4)", "package_ndc": "71335-2052-4", "marketing_start_date": "20220216"}, {"sample": false, "description": "45 TABLET, COATED in 1 BOTTLE (71335-2052-5)", "package_ndc": "71335-2052-5", "marketing_start_date": "20220318"}, {"sample": false, "description": "58 TABLET, COATED in 1 BOTTLE (71335-2052-6)", "package_ndc": "71335-2052-6", "marketing_start_date": "20220318"}, {"sample": false, "description": "18 TABLET, COATED in 1 BOTTLE (71335-2052-7)", "package_ndc": "71335-2052-7", "marketing_start_date": "20220318"}, {"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (71335-2052-8)", "package_ndc": "71335-2052-8", "marketing_start_date": "20220318"}], "brand_name": "Diclofenac Potassium", "product_id": "71335-2052_5c0968a7-d80a-4a70-8e03-6a88d72c2545", "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": "71335-2052", "generic_name": "diclofenac potassium", "labeler_name": "Bryant Ranch Prepack", "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"}