diclofenac sodium
Generic: diclofenac sodium
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac sodium
Labeler
proficient rx lp
Dosage Form
SOLUTION
Routes
Active Ingredients
diclofenac sodium 16.05 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71205-062
Product ID
71205-062_d8f31daf-5694-4d1a-babd-bb02b951173a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203818
Listing Expiration
2026-12-31
Marketing Start
2014-11-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205062
Hyphenated Format
71205-062
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
ANDA203818 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 16.05 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (71205-062-15) / 150 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d8f31daf-5694-4d1a-babd-bb02b951173a", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["b0f9e649-6651-406f-a9fe-157fe04d9d27"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (71205-062-15) / 150 mL in 1 BOTTLE, DROPPER", "package_ndc": "71205-062-15", "marketing_start_date": "20180702"}], "brand_name": "Diclofenac sodium", "product_id": "71205-062_d8f31daf-5694-4d1a-babd-bb02b951173a", "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": "71205-062", "generic_name": "diclofenac sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA203818", "marketing_category": "ANDA", "marketing_start_date": "20141126", "listing_expiration_date": "20261231"}