diclofenac sodium
Generic: diclofenac sodium
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
diclofenac sodium
Generic Name
diclofenac sodium
Labeler
a-s medication solutions
Dosage Form
SOLUTION
Routes
Active Ingredients
diclofenac sodium 16.05 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6713
Product ID
50090-6713_26ba1718-9a11-4c8f-b16f-88106755915c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203818
Listing Expiration
2026-12-31
Marketing Start
2014-11-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906713
Hyphenated Format
50090-6713
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
ANDA203818 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 16.05 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (50090-6713-0) / 150 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "26ba1718-9a11-4c8f-b16f-88106755915c", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["0379c918-1717-40ab-81cc-268116950fd5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (50090-6713-0) / 150 mL in 1 BOTTLE, DROPPER", "package_ndc": "50090-6713-0", "marketing_start_date": "20231002"}], "brand_name": "Diclofenac Sodium", "product_id": "50090-6713_26ba1718-9a11-4c8f-b16f-88106755915c", "dosage_form": "SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-6713", "generic_name": "Diclofenac Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA203818", "marketing_category": "ANDA", "marketing_start_date": "20141126", "listing_expiration_date": "20261231"}