diclofenac sodium
Generic: diclofenac
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac
Labeler
preferred pharmaceuticals inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
diclofenac sodium 16.05 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7270
Product ID
68788-7270_ff81467f-1bc6-433c-9119-a4e9b1ab0011
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206116
Listing Expiration
2026-12-31
Marketing Start
2019-01-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887270
Hyphenated Format
68788-7270
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 (source: ndc)
Application Number
ANDA206116 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 16.05 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (68788-7270-1) / 150 mL 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": "ff81467f-1bc6-433c-9119-a4e9b1ab0011", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["937e9ba5-cdad-4e72-a77a-bad699e1b236"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68788-7270-1) / 150 mL in 1 BOTTLE", "package_ndc": "68788-7270-1", "marketing_start_date": "20190111"}], "brand_name": "Diclofenac Sodium", "product_id": "68788-7270_ff81467f-1bc6-433c-9119-a4e9b1ab0011", "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": "68788-7270", "generic_name": "Diclofenac", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA206116", "marketing_category": "ANDA", "marketing_start_date": "20190111", "listing_expiration_date": "20261231"}