DermasilkRx DicloPak
Approved
Approval ID
1c948de4-dbbf-309a-e054-00144ff8d46c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 5, 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 Code69329-330
Application NumberANDA074514
Product Classification
M
Marketing Category
C73584
G
Generic Name
diclofenac sodium delayed release tablets, ranitidine tablets, capsaicin cream
Product Specifications
Effective DateAugust 5, 2015
FDA Product Classification