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Betamethasone Valerate
Betamethasone Valerate - 54879-004-60 - (Betamethasone Valerate)
Drug Information of Betamethasone Valerate
| Product NDC: | 54879-004 |
| Proprietary Name: | Betamethasone Valerate |
| Non Proprietary Name: | Betamethasone Valerate |
| Active Ingredient(s): | 1 mg/mL & nbsp; Betamethasone Valerate |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Betamethasone Valerate
| Product NDC: | 54879-004 |
| Labeler Name: | STI Pharma |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070052 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19850731 |
Package Information of Betamethasone Valerate
| Package NDC: | 54879-004-60 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (54879-004-60) > 60 mL in 1 BOTTLE, PLASTIC |
NDC Information of Betamethasone Valerate
| NDC Code | 54879-004-60 |
| Proprietary Name | Betamethasone Valerate |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (54879-004-60) > 60 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 54879-004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Betamethasone Valerate |
| Dosage Form Name | LOTION |
| Route Name | CUTANEOUS |
| Start Marketing Date | 19850731 |
| Marketing Category Name | ANDA |
| Labeler Name | STI Pharma |
| Substance Name | BETAMETHASONE VALERATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
