diclofenac sodium
Generic: diclofenac sodium
Labeler: asclemed usa, incDrug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac sodium
Labeler
asclemed usa, inc
Dosage Form
SOLUTION
Routes
Active Ingredients
diclofenac sodium 20 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
76420-861
Product ID
76420-861_239fc4df-8f2c-e524-e063-6394a90a2bae
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213040
Listing Expiration
2026-12-31
Marketing Start
2023-02-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420861
Hyphenated Format
76420-861
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
ANDA213040 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/g
Packaging
- 1 BOTTLE in 1 CARTON (76420-861-04) / 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": "239fc4df-8f2c-e524-e063-6394a90a2bae", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["1487074"], "spl_set_id": ["2e3e6de9-7e07-4df3-9fea-ac50ddcde840"], "manufacturer_name": ["Asclemed USA, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (76420-861-04) / 112 g in 1 BOTTLE", "package_ndc": "76420-861-04", "marketing_start_date": "20241004"}], "brand_name": "Diclofenac Sodium", "product_id": "76420-861_239fc4df-8f2c-e524-e063-6394a90a2bae", "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": "76420-861", "generic_name": "Diclofenac Sodium", "labeler_name": "Asclemed USA, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "20 mg/g"}], "application_number": "ANDA213040", "marketing_category": "ANDA", "marketing_start_date": "20230203", "listing_expiration_date": "20261231"}