Details for New Drug Application (NDA): 205076
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NDA 205076 describes OXICONAZOLE NITRATE, which is a drug marketed by Sun Pharma Canada and is included in one NDA. It is available from one supplier. Additional details are available on the OXICONAZOLE NITRATE profile page.
The generic ingredient in OXICONAZOLE NITRATE is oxiconazole nitrate. There are four drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the oxiconazole nitrate profile page.
The generic ingredient in OXICONAZOLE NITRATE is oxiconazole nitrate. There are four drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the oxiconazole nitrate profile page.
Summary for 205076
| Tradename: | OXICONAZOLE NITRATE |
| Applicant: | Sun Pharma Canada |
| Ingredient: | oxiconazole nitrate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 205076
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| OXICONAZOLE NITRATE | oxiconazole nitrate | CREAM;TOPICAL | 205076 | ANDA | Sun Pharmaceutical Industries, Inc. | 51672-1359 | 51672-1359-1 | 1 TUBE in 1 CARTON (51672-1359-1) / 15 g in 1 TUBE |
| OXICONAZOLE NITRATE | oxiconazole nitrate | CREAM;TOPICAL | 205076 | ANDA | Sun Pharmaceutical Industries, Inc. | 51672-1359 | 51672-1359-2 | 1 TUBE in 1 CARTON (51672-1359-2) / 30 g in 1 TUBE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CREAM;TOPICAL | Strength | EQ 1% BASE | ||||
| Approval Date: | Mar 7, 2016 | TE: | AB | RLD: | No | ||||
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