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/ DROPS
Routes
Active Ingredients
diclofenac sodium 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-2454
Product ID
50090-2454_98e8ede7-aa2f-4dfa-90de-b7a9c5b828b4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078792
Listing Expiration
2026-12-31
Marketing Start
2007-12-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500902454
Hyphenated Format
50090-2454
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
ANDA078792 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (50090-2454-0) / 5 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "98e8ede7-aa2f-4dfa-90de-b7a9c5b828b4", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["854801"], "spl_set_id": ["5d74488c-e092-415d-b19b-05318380d9b1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (50090-2454-0) / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "50090-2454-0", "marketing_start_date": "20160812"}], "brand_name": "Diclofenac Sodium", "product_id": "50090-2454_98e8ede7-aa2f-4dfa-90de-b7a9c5b828b4", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-2454", "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": "1 mg/mL"}], "application_number": "ANDA078792", "marketing_category": "ANDA", "marketing_start_date": "20071228", "listing_expiration_date": "20261231"}