diclofenac potassium
Generic: diclofenac potassium
Labeler: ascend laboratories, llcDrug Facts
Product Profile
Brand Name
diclofenac potassium
Generic Name
diclofenac potassium
Labeler
ascend laboratories, llc
Dosage Form
POWDER, FOR SOLUTION
Routes
Active Ingredients
diclofenac potassium 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67877-772
Product ID
67877-772_2b2c8805-3cf1-48f8-9612-8a72a30a7f20
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216635
Listing Expiration
2026-12-31
Marketing Start
2022-10-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67877772
Hyphenated Format
67877-772
Supplemental Identifiers
RxCUI
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
ANDA216635 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 9 PACKET in 1 CARTON (67877-772-58) / 1 POWDER, FOR SOLUTION in 1 PACKET (67877-772-49)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b2c8805-3cf1-48f8-9612-8a72a30a7f20", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["859063"], "spl_set_id": ["f675a627-c944-4ec6-8c08-b5fdb78dc269"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 PACKET in 1 CARTON (67877-772-58) / 1 POWDER, FOR SOLUTION in 1 PACKET (67877-772-49)", "package_ndc": "67877-772-58", "marketing_start_date": "20221024"}], "brand_name": "Diclofenac Potassium", "product_id": "67877-772_2b2c8805-3cf1-48f8-9612-8a72a30a7f20", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "67877-772", "generic_name": "Diclofenac Potassium", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA216635", "marketing_category": "ANDA", "marketing_start_date": "20221024", "listing_expiration_date": "20261231"}