diclofenac potassium
Generic: diclofenac potassium
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
diclofenac potassium
Generic Name
diclofenac potassium
Labeler
heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
diclofenac potassium 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
23155-840
Product ID
23155-840_c85f2a53-359f-4aa2-b103-7239798ec773
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
23155840
Hyphenated Format
23155-840
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 (23155-840-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c85f2a53-359f-4aa2-b103-7239798ec773", "openfda": {"upc": ["0323155840124"], "unii": ["L4D5UA6CB4"], "rxcui": ["858342"], "spl_set_id": ["d64537c8-e397-4d17-b95c-3092668260aa"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE, LIQUID FILLED in 1 BOTTLE (23155-840-12)", "package_ndc": "23155-840-12", "marketing_start_date": "20221121"}], "brand_name": "diclofenac potassium", "product_id": "23155-840_c85f2a53-359f-4aa2-b103-7239798ec773", "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": "23155-840", "generic_name": "diclofenac potassium", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "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"}