diclofenac sodium
Generic: diclofenac sodium
Labeler: phoenix rx llcDrug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac sodium
Labeler
phoenix rx llc
Dosage Form
SOLUTION
Routes
Active Ingredients
diclofenac sodium 20 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
85509-2406
Product ID
85509-2406_43926d0d-1675-d436-e063-6294a90a78ba
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207714
Listing Expiration
2026-12-31
Marketing Start
2022-05-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
855092406
Hyphenated Format
85509-2406
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 sodium (source: ndc)
Generic Name
diclofenac sodium (source: ndc)
Application Number
ANDA207714 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/g
Packaging
- 1 BOTTLE in 1 CARTON (85509-2406-1) / 112 g in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "43926d0d-1675-d436-e063-6294a90a78ba", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["1487074"], "spl_set_id": ["4382cc15-8978-4f3b-e063-6394a90a9ecb"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (85509-2406-1) / 112 g in 1 BOTTLE", "package_ndc": "85509-2406-1", "marketing_start_date": "20251114"}], "brand_name": "Diclofenac Sodium", "product_id": "85509-2406_43926d0d-1675-d436-e063-6294a90a78ba", "dosage_form": "SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "85509-2406", "generic_name": "Diclofenac Sodium", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "20 mg/g"}], "application_number": "ANDA207714", "marketing_category": "ANDA", "marketing_start_date": "20220509", "listing_expiration_date": "20261231"}