arthritis pain reliever
Generic: diclofenac sodium
Labeler: h e bDrug Facts
Product Profile
Brand Name
arthritis pain reliever
Generic Name
diclofenac sodium
Labeler
h e b
Dosage Form
GEL
Routes
Active Ingredients
diclofenac sodium 10 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
59640-198
Product ID
59640-198_45a40aa3-3eb2-4f37-b9f0-990f7836193e
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA211253
Listing Expiration
2026-12-31
Marketing Start
2025-04-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59640198
Hyphenated Format
59640-198
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
arthritis pain reliever (source: ndc)
Generic Name
diclofenac sodium (source: ndc)
Application Number
ANDA211253 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/g
Packaging
- 1 TUBE in 1 CARTON (59640-198-01) / 100 g in 1 TUBE
- 1 TUBE in 1 CARTON (59640-198-02) / 50 g in 1 TUBE
- 1 TUBE in 1 CARTON (59640-198-03) / 150 g in 1 TUBE
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "45a40aa3-3eb2-4f37-b9f0-990f7836193e", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["027803c5-85ae-4b86-8bd4-e61f8f34d036"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (59640-198-01) / 100 g in 1 TUBE", "package_ndc": "59640-198-01", "marketing_start_date": "20250718"}, {"sample": false, "description": "1 TUBE in 1 CARTON (59640-198-02) / 50 g in 1 TUBE", "package_ndc": "59640-198-02", "marketing_start_date": "20250916"}, {"sample": false, "description": "1 TUBE in 1 CARTON (59640-198-03) / 150 g in 1 TUBE", "package_ndc": "59640-198-03", "marketing_start_date": "20250422"}], "brand_name": "ARTHRITIS PAIN RELIEVER", "product_id": "59640-198_45a40aa3-3eb2-4f37-b9f0-990f7836193e", "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": "59640-198", "generic_name": "DICLOFENAC SODIUM", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ARTHRITIS PAIN RELIEVER", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA211253", "marketing_category": "ANDA", "marketing_start_date": "20250422", "listing_expiration_date": "20261231"}