diclofenac potassium
Generic: diclofenac potassium
Labeler: amici pharma inc.Drug Facts
Product Profile
Brand Name
diclofenac potassium
Generic Name
diclofenac potassium
Labeler
amici pharma inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
diclofenac potassium 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69292-548
Product ID
69292-548_cf4973de-8da2-4fdf-8f48-938627e09d5a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076561
Listing Expiration
2026-12-31
Marketing Start
2024-04-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69292548
Hyphenated Format
69292-548
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA076561 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69292-548-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cf4973de-8da2-4fdf-8f48-938627e09d5a", "openfda": {"upc": ["0369292548301"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942", "857702"], "spl_set_id": ["f2908870-a517-491f-8771-4100d11b4b64"], "manufacturer_name": ["Amici Pharma Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69292-548-30)", "package_ndc": "69292-548-30", "marketing_start_date": "20240418"}], "brand_name": "Diclofenac Potassium", "product_id": "69292-548_cf4973de-8da2-4fdf-8f48-938627e09d5a", "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": "69292-548", "generic_name": "diclofenac potassium", "labeler_name": "Amici Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA076561", "marketing_category": "ANDA", "marketing_start_date": "20240418", "listing_expiration_date": "20261231"}