diclofenac potassium

Generic: diclofenac potassium

Labeler: taro pharmaceuticals u.s.a., inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler taro pharmaceuticals u.s.a., inc.
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

diclofenac potassium 50 mg/1

Manufacturer
Taro Pharmaceuticals U.S.A., Inc.

Identifiers & Regulatory

Product NDC 51672-4240
Product ID 51672-4240_24354f73-c3f7-12fa-e063-6294a90ac338
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218011
Listing Expiration 2026-12-31
Marketing Start 2024-06-24

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 516724240
Hyphenated Format 51672-4240

Supplemental Identifiers

RxCUI
859063
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 ANDA218011 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 9 PACKET in 1 CARTON (51672-4240-6) / 1 POWDER, FOR SOLUTION in 1 PACKET (51672-4240-8)
source: ndc

Packages (1)

Ingredients (1)

diclofenac potassium (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24354f73-c3f7-12fa-e063-6294a90ac338", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["859063"], "spl_set_id": ["68a926a2-b818-420f-9c9a-fd91dc5a8f36"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 PACKET in 1 CARTON (51672-4240-6)  / 1 POWDER, FOR SOLUTION in 1 PACKET (51672-4240-8)", "package_ndc": "51672-4240-6", "marketing_start_date": "20240624"}], "brand_name": "Diclofenac Potassium", "product_id": "51672-4240_24354f73-c3f7-12fa-e063-6294a90ac338", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51672-4240", "generic_name": "Diclofenac Potassium", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA218011", "marketing_category": "ANDA", "marketing_start_date": "20240624", "listing_expiration_date": "20261231"}