diclofenac sodium

Generic: diclofenac sodium

Labeler: redpharm drug, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac sodium
Generic Name diclofenac sodium
Labeler redpharm drug, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

diclofenac sodium 75 mg/1

Manufacturer
RedPharm Drug, Inc.

Identifiers & Regulatory

Product NDC 67296-1197
Product ID 67296-1197_3252d443-e09c-9209-e063-6294a90a5b2e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075185
Listing Expiration 2026-12-31
Marketing Start 1998-11-13

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 672961197
Hyphenated Format 67296-1197

Supplemental Identifiers

RxCUI
855926
UPC
0367296119725
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 ANDA075185 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 20 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-2)
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-3)
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-6)
source: ndc

Packages (3)

67296-1197-2 20 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-2) 67296-1197-3 30 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-3) 67296-1197-6 60 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-6)

Ingredients (1)

diclofenac sodium (75 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": "3252d443-e09c-9209-e063-6294a90a5b2e", "openfda": {"upc": ["0367296119725"], "unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["4ecb7bdc-4a5e-7444-e054-00144ff88e88"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-2)", "package_ndc": "67296-1197-2", "marketing_start_date": "19981113"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-3)", "package_ndc": "67296-1197-3", "marketing_start_date": "19981113"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1197-6)", "package_ndc": "67296-1197-6", "marketing_start_date": "19981113"}], "brand_name": "Diclofenac Sodium", "product_id": "67296-1197_3252d443-e09c-9209-e063-6294a90a5b2e", "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": "67296-1197", "generic_name": "Diclofenac Sodium", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "19981113", "listing_expiration_date": "20261231"}