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Avita - 0378-6141-44 - (tretinoin)
Drug Information of Avita
| Product NDC: | 0378-6141 |
| Proprietary Name: | Avita |
| Non Proprietary Name: | tretinoin |
| Active Ingredient(s): | .25 mg/g & nbsp; tretinoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Avita
| Product NDC: | 0378-6141 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020404 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110520 |
Package Information of Avita
| Package NDC: | 0378-6141-44 |
| Package Description: | 20 g in 1 TUBE (0378-6141-44) |
NDC Information of Avita
| NDC Code | 0378-6141-44 |
| Proprietary Name | Avita |
| Package Description | 20 g in 1 TUBE (0378-6141-44) |
| Product NDC | 0378-6141 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tretinoin |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110520 |
| Marketing Category Name | NDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | TRETINOIN |
| Strength Number | .25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
