diclofenac potassium

Generic: diclofenac potassium

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac potassium
Generic Name diclofenac potassium
Labeler ascend laboratories, llc
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

diclofenac potassium 50 mg/1

Manufacturer
Ascend Laboratories, LLC

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
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 67877772
Hyphenated Format 67877-772

Supplemental Identifiers

RxCUI
859063
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 ANDA216635 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 9 PACKET in 1 CARTON (67877-772-58) / 1 POWDER, FOR SOLUTION in 1 PACKET (67877-772-49)
source: ndc

Packages (1)

Ingredients (1)

diclofenac potassium (50 mg/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"}