diclofenac sodium
Generic: diclofenac sodium
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac sodium
Labeler
preferred pharmaceuticals inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
diclofenac sodium 20 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8743
Product ID
68788-8743_88b382bf-aa30-4c2e-98b0-c360e1427119
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208021
Listing Expiration
2026-12-31
Marketing Start
2024-09-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888743
Hyphenated Format
68788-8743
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
ANDA208021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/g
Packaging
- 1 BOTTLE, PUMP in 1 CARTON (68788-8743-1) / 112 g in 1 BOTTLE, PUMP
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "88b382bf-aa30-4c2e-98b0-c360e1427119", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["1487074"], "spl_set_id": ["e042e64c-5f18-4483-bcbd-dfd9b08a81cf"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PUMP in 1 CARTON (68788-8743-1) / 112 g in 1 BOTTLE, PUMP", "package_ndc": "68788-8743-1", "marketing_start_date": "20240926"}], "brand_name": "Diclofenac Sodium", "product_id": "68788-8743_88b382bf-aa30-4c2e-98b0-c360e1427119", "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": "68788-8743", "generic_name": "Diclofenac Sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "20 mg/g"}], "application_number": "ANDA208021", "marketing_category": "ANDA", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}