diclofenac sodium
Generic: diclofenac sodium
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac sodium
Labeler
asclemed usa, inc.
Dosage Form
GEL
Routes
Active Ingredients
diclofenac sodium 30 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
76420-275
Product ID
76420-275_e83802ce-a8c7-e6a6-e053-2995a90a5256
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206298
Listing Expiration
2026-12-31
Marketing Start
2016-04-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420275
Hyphenated Format
76420-275
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
ANDA206298 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/g
Packaging
- 100 g in 1 TUBE (76420-275-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "e83802ce-a8c7-e6a6-e053-2995a90a5256", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["d4b81a74-6926-4715-bf90-aec026cff2b4"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 g in 1 TUBE (76420-275-01)", "package_ndc": "76420-275-01", "marketing_start_date": "20220909"}], "brand_name": "Diclofenac sodium", "product_id": "76420-275_e83802ce-a8c7-e6a6-e053-2995a90a5256", "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": "76420-275", "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": "30 mg/g"}], "application_number": "ANDA206298", "marketing_category": "ANDA", "marketing_start_date": "20160428", "listing_expiration_date": "20261231"}