Product NDC: | 63481-684 |
Proprietary Name: | Voltaren |
Non Proprietary Name: | diclofenac sodium |
Active Ingredient(s): | 10 mg/g & nbsp; diclofenac sodium |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63481-684 |
Labeler Name: | Endo Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022122 |
Marketing Category: | NDA |
Start Marketing Date: | 20071017 |
Package NDC: | 63481-684-83 |
Package Description: | 1 TUBE in 1 CARTON (63481-684-83) > 20 g in 1 TUBE |
NDC Code | 63481-684-83 |
Proprietary Name | Voltaren |
Package Description | 1 TUBE in 1 CARTON (63481-684-83) > 20 g in 1 TUBE |
Product NDC | 63481-684 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | diclofenac sodium |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20071017 |
Marketing Category Name | NDA |
Labeler Name | Endo Pharmaceuticals, Inc. |
Substance Name | DICLOFENAC SODIUM |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |