diclofenac potassium
Generic: diclofenac potassium
Labeler: ina pharmaceutics incDrug Facts
Product Profile
Brand Name
diclofenac potassium
Generic Name
diclofenac potassium
Labeler
ina pharmaceutics inc
Dosage Form
TABLET, COATED
Routes
Active Ingredients
diclofenac potassium 25 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
74157007
Hyphenated Format
74157-007
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 60 TABLET, COATED in 1 BOTTLE (74157-007-60)
Packages (1)
Ingredients (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"}