Product NDC: | 16590-034 |
Proprietary Name: | BETAMETHASONE VALERATE |
Non Proprietary Name: | BETAMETHASONE VALERATE |
Active Ingredient(s): | 1 mg/g & nbsp; BETAMETHASONE VALERATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-034 |
Labeler Name: | STAT RX USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA018861 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091023 |
Package NDC: | 16590-034-45 |
Package Description: | 45 g in 1 TUBE (16590-034-45) |
NDC Code | 16590-034-45 |
Proprietary Name | BETAMETHASONE VALERATE |
Package Description | 45 g in 1 TUBE (16590-034-45) |
Product NDC | 16590-034 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | BETAMETHASONE VALERATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20091023 |
Marketing Category Name | ANDA |
Labeler Name | STAT RX USA LLC |
Substance Name | BETAMETHASONE VALERATE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |