Diclofenac Potassium
Diclofenac Potassium Tablets, USP 25 mg
Approved
Approval ID
bce95bb3-3097-4e7d-8d29-0870bb729212
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 8, 2023
Manufacturers
FDA
CARWIN PHARMACEUTICAL ASSOCIATES, LLC
DUNS: 079217215
FDA
Carwin Pharmaceutical Associates, LLC
DUNS: 079217215
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
DICLOFENAC POTASSIUM
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code15370-185
Application NumberANDA076561
Product Classification
M
Marketing Category
C73584
G
Generic Name
DICLOFENAC POTASSIUM
Product Specifications
Route of AdministrationORAL
Effective DateNovember 8, 2023
FDA Product Classification
INGREDIENTS (1)
DICLOFENAC POTASSIUMActive
Quantity: 25 mg in 1 1
Code: L4D5UA6CB4
Classification: ACTIB