diclofenac potassium

Generic: diclofenac potassium

Labeler: ina pharmaceutics inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler ina pharmaceutics inc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diclofenac potassium 25 mg/1

Manufacturer
INA Pharmaceutics Inc

Identifiers & Regulatory

Product NDC 74157-007
Product ID 74157-007_4081e948-870f-7c20-e063-6294a90a9184
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075229
Listing Expiration 2026-12-31
Marketing Start 2021-09-20

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 74157007
Hyphenated Format 74157-007

Supplemental Identifiers

RxCUI
857702
UPC
0374157007602
UNII
L4D5UA6CB4

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 potassium (source: ndc)
Generic Name diclofenac potassium (source: ndc)
Application Number ANDA075229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 60 TABLET, COATED in 1 BOTTLE (74157-007-60)
source: ndc

Packages (1)

Ingredients (1)

diclofenac potassium (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4081e948-870f-7c20-e063-6294a90a9184", "openfda": {"upc": ["0374157007602"], "unii": ["L4D5UA6CB4"], "rxcui": ["857702"], "spl_set_id": ["5ecd99fe-cb74-4a65-9636-2aefd2416ece"], "manufacturer_name": ["INA Pharmaceutics Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (74157-007-60)", "package_ndc": "74157-007-60", "marketing_start_date": "20210920"}], "brand_name": "Diclofenac Potassium", "product_id": "74157-007_4081e948-870f-7c20-e063-6294a90a9184", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "74157-007", "generic_name": "diclofenac potassium", "labeler_name": "INA Pharmaceutics Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA075229", "marketing_category": "ANDA", "marketing_start_date": "20210920", "listing_expiration_date": "20261231"}