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Betamethasone Valerate
Betamethasone Valerate - 0093-0671-39 - (Betamethasone Valerate)
Drug Information of Betamethasone Valerate
| Product NDC: | 0093-0671 |
| Proprietary Name: | Betamethasone Valerate |
| Non Proprietary Name: | Betamethasone Valerate |
| Active Ingredient(s): | 1 mg/mL & nbsp; Betamethasone Valerate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Betamethasone Valerate
| Product NDC: | 0093-0671 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070072 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900930 |
Package Information of Betamethasone Valerate
| Package NDC: | 0093-0671-39 |
| Package Description: | 60 mL in 1 BOTTLE, PLASTIC (0093-0671-39) |
NDC Information of Betamethasone Valerate
| NDC Code | 0093-0671-39 |
| Proprietary Name | Betamethasone Valerate |
| Package Description | 60 mL in 1 BOTTLE, PLASTIC (0093-0671-39) |
| Product NDC | 0093-0671 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Betamethasone Valerate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19900930 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | BETAMETHASONE VALERATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
