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Betamethasone Dipropionate
Betamethasone Dipropionate - 0781-7074-50 - (Betamethasone Dipropionate)
Drug Information of Betamethasone Dipropionate
| Product NDC: | 0781-7074 |
| 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) |
Labeler Information of Betamethasone Dipropionate
| Product NDC: | 0781-7074 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076603 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040123 |
Package Information of Betamethasone Dipropionate
| Package NDC: | 0781-7074-50 |
| Package Description: | 50 g in 1 TUBE (0781-7074-50) |
NDC Information of Betamethasone Dipropionate
| NDC Code | 0781-7074-50 |
| Proprietary Name | Betamethasone Dipropionate |
| Package Description | 50 g in 1 TUBE (0781-7074-50) |
| Product NDC | 0781-7074 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Betamethasone Dipropionate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20040123 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | BETAMETHASONE DIPROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
