diclofenac sodium

Generic: diclofenac sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac sodium
Generic Name diclofenac sodium
Labeler a-s medication solutions
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

diclofenac sodium 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0541
Product ID 50090-0541_6e6bf250-49a3-464a-9835-ae8160eaac05
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090066
Listing Expiration 2027-12-31
Marketing Start 2010-12-31

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] decreased prostaglandin production [pe] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500900541
Hyphenated Format 50090-0541

Supplemental Identifiers

RxCUI
855906 855926
UNII
QTG126297Q

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 ANDA090066 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0541-0)
  • 14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0541-1)
source: ndc

Packages (2)

50090-0541-0 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0541-0) 50090-0541-1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0541-1)

Ingredients (1)

diclofenac sodium (50 mg/1)

Linked Drug Pages (1)

Diclofenac Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6e6bf250-49a3-464a-9835-ae8160eaac05", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906", "855926"], "spl_set_id": ["1e669fc2-69bf-4439-a336-a103e5b9cafe"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0541-0)", "package_ndc": "50090-0541-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0541-1)", "package_ndc": "50090-0541-1", "marketing_start_date": "20141128"}], "brand_name": "Diclofenac Sodium", "product_id": "50090-0541_6e6bf250-49a3-464a-9835-ae8160eaac05", "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": "50090-0541", "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": "50 mg/1"}], "application_number": "ANDA090066", "marketing_category": "ANDA", "marketing_start_date": "20101231", "listing_expiration_date": "20271231"}