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Betamethasone
Betamethasone - 0115-1472-56 - (Betamethasone)
Drug Information of Betamethasone
| Product NDC: | 0115-1472 |
| Proprietary Name: | Betamethasone |
| Non Proprietary Name: | Betamethasone |
| Active Ingredient(s): | .5 mg/g & nbsp; Betamethasone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Betamethasone
| Product NDC: | 0115-1472 |
| Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076603 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040123 |
Package Information of Betamethasone
| Package NDC: | 0115-1472-56 |
| Package Description: | 1 TUBE in 1 CARTON (0115-1472-56) > 50 g in 1 TUBE |
NDC Information of Betamethasone
| NDC Code | 0115-1472-56 |
| Proprietary Name | Betamethasone |
| Package Description | 1 TUBE in 1 CARTON (0115-1472-56) > 50 g in 1 TUBE |
| Product NDC | 0115-1472 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Betamethasone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20040123 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Substance Name | BETAMETHASONE DIPROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
