diclofenac potassium

Generic: diclofenac potassium tablets

Labeler: zydus pharmaceuticals (usa) inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium tablets
Labeler zydus pharmaceuticals (usa) inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diclofenac potassium 50 mg/1

Manufacturer
Zydus Pharmaceuticals (USA) Inc.

Identifiers & Regulatory

Product NDC 70710-1832
Product ID 70710-1832_47dd2b04-1417-2e67-e063-6294a90ae24b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215750
Listing Expiration 2027-12-31
Marketing Start 2022-05-12

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 707101832
Hyphenated Format 70710-1832

Supplemental Identifiers

RxCUI
855942
UPC
0370710183202
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 tablets (source: ndc)
Application Number ANDA215750 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1832-0)
  • 100 TABLET, FILM COATED in 1 BOTTLE (70710-1832-1)
  • 500 TABLET, FILM COATED in 1 BOTTLE (70710-1832-5)
source: ndc

Packages (3)

70710-1832-0 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1832-0) 70710-1832-1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1832-1) 70710-1832-5 500 TABLET, FILM COATED in 1 BOTTLE (70710-1832-5)

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": "47dd2b04-1417-2e67-e063-6294a90ae24b", "openfda": {"upc": ["0370710183202"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["1aa3d8d6-dd1c-46c7-96f9-2b5c9d72764a"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (70710-1832-0)", "package_ndc": "70710-1832-0", "marketing_start_date": "20220512"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1832-1)", "package_ndc": "70710-1832-1", "marketing_start_date": "20220512"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70710-1832-5)", "package_ndc": "70710-1832-5", "marketing_start_date": "20220512"}], "brand_name": "Diclofenac Potassium", "product_id": "70710-1832_47dd2b04-1417-2e67-e063-6294a90ae24b", "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": "70710-1832", "generic_name": "Diclofenac Potassium Tablets", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA215750", "marketing_category": "ANDA", "marketing_start_date": "20220512", "listing_expiration_date": "20271231"}