| Product NDC: | 49999-222 | 
| Proprietary Name: | Betamethasone Dipropionate | 
| Non Proprietary Name: | Betamethasone Dipropionate | 
| Active Ingredient(s): | .5 mg/g & nbsp; Betamethasone Dipropionate | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | CREAM | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 49999-222 | 
| Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA019137 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20120326 | 
| Package NDC: | 49999-222-45 | 
| Package Description: | 1 TUBE in 1 CARTON (49999-222-45) > 45 g in 1 TUBE | 
| NDC Code | 49999-222-45 | 
| Proprietary Name | Betamethasone Dipropionate | 
| Package Description | 1 TUBE in 1 CARTON (49999-222-45) > 45 g in 1 TUBE | 
| Product NDC | 49999-222 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Betamethasone Dipropionate | 
| Dosage Form Name | CREAM | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20120326 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 
| Substance Name | BETAMETHASONE DIPROPIONATE | 
| Strength Number | .5 | 
| Strength Unit | mg/g | 
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |