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
GEL
Routes
Active Ingredients
diclofenac sodium 30 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8237
Product ID
68788-8237_488f67d7-bbdd-44fd-bd37-20ce051d5970
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210893
Listing Expiration
2026-12-31
Marketing Start
2022-08-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888237
Hyphenated Format
68788-8237
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
ANDA210893 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/g
Packaging
- 1 TUBE in 1 CARTON (68788-8237-1) / 100 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "488f67d7-bbdd-44fd-bd37-20ce051d5970", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["632f553b-130a-4d45-8dcd-fe6fcf6a9ab8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68788-8237-1) / 100 g in 1 TUBE", "package_ndc": "68788-8237-1", "marketing_start_date": "20220809"}], "brand_name": "diclofenac sodium", "product_id": "68788-8237_488f67d7-bbdd-44fd-bd37-20ce051d5970", "dosage_form": "GEL", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8237", "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": "30 mg/g"}], "application_number": "ANDA210893", "marketing_category": "ANDA", "marketing_start_date": "20220809", "listing_expiration_date": "20261231"}