diclofenac sodium delayed release
Generic: diclofenac sodium
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
diclofenac sodium delayed release
Generic Name
diclofenac sodium
Labeler
a-s medication solutions
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
diclofenac sodium 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-0543
Product ID
50090-0543_02eb3aca-0433-4c56-818d-cd8501244b84
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075185
Listing Expiration
2026-12-31
Marketing Start
1998-11-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500900543
Hyphenated Format
50090-0543
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 delayed release (source: ndc)
Generic Name
diclofenac sodium (source: ndc)
Application Number
ANDA075185 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0543-0)
- 14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0543-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "02eb3aca-0433-4c56-818d-cd8501244b84", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["9df87100-acf5-4b46-93b4-067b470136bd"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0543-0)", "package_ndc": "50090-0543-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0543-1)", "package_ndc": "50090-0543-1", "marketing_start_date": "20141128"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "50090-0543_02eb3aca-0433-4c56-818d-cd8501244b84", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-0543", "generic_name": "Diclofenac Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "19981113", "listing_expiration_date": "20261231"}