diclofenac potassium

Generic: diclofenac potassium

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

diclofenac potassium 50 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-0948
Product ID 0093-0948_b9f656e7-0a32-460d-9c86-8065a7f4b108
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 00930948
Hyphenated Format 0093-0948

Supplemental Identifiers

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

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0093-0948-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (0093-0948-05)
source: ndc

Packages (2)

0093-0948-01 100 TABLET, FILM COATED in 1 BOTTLE (0093-0948-01) 0093-0948-05 500 TABLET, FILM COATED in 1 BOTTLE (0093-0948-05)

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": "b9f656e7-0a32-460d-9c86-8065a7f4b108", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["77b60a0c-e49a-4ad4-abb1-b662c24ab782"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-0948-01)", "package_ndc": "0093-0948-01", "marketing_start_date": "19980811"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0093-0948-05)", "package_ndc": "0093-0948-05", "marketing_start_date": "19980811"}], "brand_name": "Diclofenac Potassium", "product_id": "0093-0948_b9f656e7-0a32-460d-9c86-8065a7f4b108", "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": "0093-0948", "generic_name": "Diclofenac Potassium", "labeler_name": "Teva Pharmaceuticals USA, 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"}