diclofenac sodium
Generic: diclofenac sodium
Labeler: nucare pharmaceuticals, llc.Drug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac sodium
Labeler
nucare pharmaceuticals, llc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
diclofenac sodium 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3720
Product ID
68071-3720_26e44fd4-d1af-d404-e063-6394a90a923d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076201
Listing Expiration
2026-12-31
Marketing Start
2002-11-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713720
Hyphenated Format
68071-3720
Supplemental Identifiers
RxCUI
UPC
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
ANDA076201 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3720-7)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "26e44fd4-d1af-d404-e063-6394a90a923d", "openfda": {"upc": ["0368071372076"], "unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["26e44aa5-cfcd-f10b-e063-6394a90a4dcf"], "manufacturer_name": ["NuCare Pharmaceuticals, LLC."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3720-7)", "package_ndc": "68071-3720-7", "marketing_start_date": "20241114"}], "brand_name": "Diclofenac Sodium", "product_id": "68071-3720_26e44fd4-d1af-d404-e063-6394a90a923d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-3720", "generic_name": "Diclofenac Sodium", "labeler_name": "NuCare Pharmaceuticals, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA076201", "marketing_category": "ANDA", "marketing_start_date": "20021106", "listing_expiration_date": "20261231"}