DeramsilkRx Anodynexa Pak
Approved
Approval ID
1b49b08b-8494-3f71-e054-00144ff88e88
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 13, 2015
Manufacturers
FDA
Patchwerx Labs, Inc.
DUNS: 079584480
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
diclofenac sodium delayed release tablets, ranitidine tablets, capsaicin cream
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69329-310
Application NumberANDA074514
Product Classification
M
Marketing Category
C73584
G
Generic Name
diclofenac sodium delayed release tablets, ranitidine tablets, capsaicin cream
Product Specifications
Effective DateJuly 13, 2015
FDA Product Classification