diclofenac sodium
Generic: diclofenac sodium
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac sodium
Labeler
remedyrepack inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
diclofenac sodium 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4044
Product ID
70518-4044_377909b0-0bfd-8e16-e063-6394a90a5f5f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216275
Listing Expiration
2026-12-31
Marketing Start
2024-04-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184044
Hyphenated Format
70518-4044
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
ANDA216275 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4044-0)
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4044-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "377909b0-0bfd-8e16-e063-6394a90a5f5f", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["6980431d-4a2b-41e9-ae86-d46b4513f04b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4044-0)", "package_ndc": "70518-4044-0", "marketing_start_date": "20240405"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4044-1)", "package_ndc": "70518-4044-1", "marketing_start_date": "20250613"}], "brand_name": "Diclofenac sodium", "product_id": "70518-4044_377909b0-0bfd-8e16-e063-6394a90a5f5f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70518-4044", "generic_name": "diclofenac sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA216275", "marketing_category": "ANDA", "marketing_start_date": "20240405", "listing_expiration_date": "20261231"}