diclofenac potassium
Generic: diclofenac potassium
Labeler: taro pharmaceuticals u.s.a., inc.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
Active Ingredients
diclofenac potassium 50 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516724240
Hyphenated Format
51672-4240
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 9 PACKET in 1 CARTON (51672-4240-6) / 1 POWDER, FOR SOLUTION in 1 PACKET (51672-4240-8)
Packages (1)
Ingredients (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"}