Product NDC: | 49999-593 |
Proprietary Name: | Diclofenac Potassium |
Non Proprietary Name: | diclofenac potassium |
Active Ingredient(s): | 50 mg/1 & nbsp; diclofenac potassium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49999-593 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075463 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111205 |
Package NDC: | 49999-593-60 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (49999-593-60) |
NDC Code | 49999-593-60 |
Proprietary Name | Diclofenac Potassium |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (49999-593-60) |
Product NDC | 49999-593 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | diclofenac potassium |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20111205 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | DICLOFENAC POTASSIUM |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |