Product NDC: | 50436-0310 |
Proprietary Name: | PENNSAID |
Non Proprietary Name: | diclofenac sodium |
Active Ingredient(s): | 16.05 mg/mL & nbsp; diclofenac sodium |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50436-0310 |
Labeler Name: | Unit Dose Services |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020947 |
Marketing Category: | NDA |
Start Marketing Date: | 20100405 |
Package NDC: | 50436-0310-1 |
Package Description: | 150 mL in 1 BOTTLE, DROPPER (50436-0310-1) |
NDC Code | 50436-0310-1 |
Proprietary Name | PENNSAID |
Package Description | 150 mL in 1 BOTTLE, DROPPER (50436-0310-1) |
Product NDC | 50436-0310 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | diclofenac sodium |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100405 |
Marketing Category Name | NDA |
Labeler Name | Unit Dose Services |
Substance Name | DICLOFENAC SODIUM |
Strength Number | 16.05 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |