diclofenac potassium
Generic: diclofenac potassium
Labeler: teva pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
diclofenac potassium
Generic Name
diclofenac potassium
Labeler
teva pharmaceuticals, inc.
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
diclofenac potassium 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0480-9435
Product ID
0480-9435_40461510-7592-d588-e063-6394a90a8b9e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204648
Listing Expiration
2026-12-31
Marketing Start
2022-03-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04809435
Hyphenated Format
0480-9435
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
ANDA204648 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (0480-9435-89)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40461510-7592-d588-e063-6394a90a8b9e", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["858342"], "spl_set_id": ["d9685883-9d0b-81da-e053-2a95a90ab8d8"], "manufacturer_name": ["TEVA PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE, LIQUID FILLED in 1 BOTTLE (0480-9435-89)", "package_ndc": "0480-9435-89", "marketing_start_date": "20220324"}], "brand_name": "Diclofenac potassium", "product_id": "0480-9435_40461510-7592-d588-e063-6394a90a8b9e", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0480-9435", "generic_name": "diclofenac potassium", "labeler_name": "TEVA PHARMACEUTICALS, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA204648", "marketing_category": "ANDA", "marketing_start_date": "20220324", "listing_expiration_date": "20261231"}