diclofenac sodium

Generic: diclofenac sodium

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac sodium
Generic Name diclofenac sodium
Labeler northstar rx llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

diclofenac sodium 25 mg/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 72603-600
Product ID 72603-600_33965722-896c-cca3-e063-6394a90a3c61
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216548
Listing Expiration 2026-12-31
Marketing Start 2025-04-23

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 72603600
Hyphenated Format 72603-600

Supplemental Identifiers

RxCUI
855664 855906 855926
UPC
0372603604030 0372603604023 0372603600018 0372603601015 0372603604016
UNII
QTG126297Q

Packaging Origin

Original Packager
true

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 ANDA216548 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-600-01)
source: ndc

Packages (1)

Ingredients (1)

diclofenac sodium (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "33965722-896c-cca3-e063-6394a90a3c61", "openfda": {"upc": ["0372603604030", "0372603604023", "0372603600018", "0372603601015", "0372603604016"], "unii": ["QTG126297Q"], "rxcui": ["855664", "855906", "855926"], "spl_set_id": ["c7431496-c0ef-403a-9716-92d942709b3d"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-600-01)", "package_ndc": "72603-600-01", "marketing_start_date": "20250423"}], "brand_name": "Diclofenac Sodium", "product_id": "72603-600_33965722-896c-cca3-e063-6394a90a3c61", "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": "72603-600", "generic_name": "Diclofenac Sodium", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "25 mg/1"}], "application_number": "ANDA216548", "marketing_category": "ANDA", "marketing_start_date": "20250423", "listing_expiration_date": "20261231"}