diclofenac sodium
Generic: diclofenac sodium
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac sodium
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
diclofenac sodium 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3556
Product ID
68071-3556_2d3fc030-5d55-2acd-e063-6294a90a11ab
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
680713556
Hyphenated Format
68071-3556
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, PLASTIC (68071-3556-7)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d3fc030-5d55-2acd-e063-6294a90a11ab", "openfda": {"upc": ["0368071355673"], "unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["0d1d19e5-4ffe-af95-e063-6394a90a7abf"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-3556-7)", "package_ndc": "68071-3556-7", "marketing_start_date": "20231222"}], "brand_name": "Diclofenac Sodium", "product_id": "68071-3556_2d3fc030-5d55-2acd-e063-6294a90a11ab", "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": "68071-3556", "generic_name": "Diclofenac Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}