Product NDC: | 0078-0478 |
Proprietary Name: | VOLTAREN |
Non Proprietary Name: | diclofenac sodium |
Active Ingredient(s): | 1 mg/mL & nbsp; diclofenac sodium |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0078-0478 |
Labeler Name: | Novartis Pharmaceutical Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020037 |
Marketing Category: | NDA |
Start Marketing Date: | 19910328 |
Package NDC: | 0078-0478-61 |
Package Description: | 5 mL in 1 BOTTLE, DROPPER (0078-0478-61) |
NDC Code | 0078-0478-61 |
Proprietary Name | VOLTAREN |
Package Description | 5 mL in 1 BOTTLE, DROPPER (0078-0478-61) |
Product NDC | 0078-0478 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | diclofenac sodium |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 19910328 |
Marketing Category Name | NDA |
Labeler Name | Novartis Pharmaceutical Corporation |
Substance Name | DICLOFENAC SODIUM |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |