diclofenac potassium
Generic: diclofenac potassium
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
diclofenac potassium
Generic Name
diclofenac potassium
Labeler
northwind health company, llc
Dosage Form
TABLET, COATED
Routes
Active Ingredients
diclofenac potassium 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-230
Product ID
51655-230_48d2c42f-dd1c-d0e8-e063-6294a90a76f7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075229
Listing Expiration
2027-12-31
Marketing Start
2022-10-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655230
Hyphenated Format
51655-230
Supplemental Identifiers
RxCUI
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
ANDA075229 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-230-52)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d2c42f-dd1c-d0e8-e063-6294a90a76f7", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["f2b6a4dd-e4e2-4acc-e053-2995a90aebf2"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-230-52)", "package_ndc": "51655-230-52", "marketing_start_date": "20221027"}], "brand_name": "Diclofenac Potassium", "product_id": "51655-230_48d2c42f-dd1c-d0e8-e063-6294a90a76f7", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51655-230", "generic_name": "diclofenac potassium", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA075229", "marketing_category": "ANDA", "marketing_start_date": "20221027", "listing_expiration_date": "20271231"}