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ERTACZO
ERTACZO - 21695-454-30 - (ERTACZO)
Drug Information of ERTACZO
| Product NDC: | 21695-454 |
| Proprietary Name: | ERTACZO |
| Non Proprietary Name: | ERTACZO |
| Active Ingredient(s): | 20 mg/g & nbsp; ERTACZO |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ERTACZO
| Product NDC: | 21695-454 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA021385 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031210 |
Package Information of ERTACZO
| Package NDC: | 21695-454-30 |
| Package Description: | 30 g in 1 TUBE (21695-454-30) |
NDC Information of ERTACZO
| NDC Code | 21695-454-30 |
| Proprietary Name | ERTACZO |
| Package Description | 30 g in 1 TUBE (21695-454-30) |
| Product NDC | 21695-454 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ERTACZO |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20031210 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | SERTACONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
