diclofenac potassium
Generic: diclofenac potassium
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
diclofenac potassium
Generic Name
diclofenac potassium
Labeler
chartwell rx, llc
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
diclofenac potassium 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62135-469
Product ID
62135-469_459be997-2951-a7cf-e063-6394a90ad491
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210078
Listing Expiration
2026-12-31
Marketing Start
2022-11-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135469
Hyphenated Format
62135-469
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
ANDA210078 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (62135-469-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459be997-2951-a7cf-e063-6394a90ad491", "openfda": {"upc": ["0362135469122"], "unii": ["L4D5UA6CB4"], "rxcui": ["858342"], "spl_set_id": ["3a837a3e-10b2-4256-b515-80c863318ccb"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE, LIQUID FILLED in 1 BOTTLE (62135-469-12)", "package_ndc": "62135-469-12", "marketing_start_date": "20230212"}], "brand_name": "Diclofenac Potassium", "product_id": "62135-469_459be997-2951-a7cf-e063-6394a90ad491", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "62135-469", "generic_name": "Diclofenac Potassium", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA210078", "marketing_category": "ANDA", "marketing_start_date": "20221121", "listing_expiration_date": "20261231"}