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TRETIN.X
TRETIN.X - 16781-376-35 - (TRETINOIN)
Drug Information of TRETIN.X
| Product NDC: | 16781-376 |
| Proprietary Name: | TRETIN.X |
| Non Proprietary Name: | TRETINOIN |
| Active Ingredient(s): | .375 mg/g & nbsp; TRETINOIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRETIN.X
| Product NDC: | 16781-376 |
| Labeler Name: | Onset Dermatologics LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090098 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130402 |
Package Information of TRETIN.X
| Package NDC: | 16781-376-35 |
| Package Description: | 1 TUBE in 1 CARTON (16781-376-35) > 35 g in 1 TUBE |
NDC Information of TRETIN.X
| NDC Code | 16781-376-35 |
| Proprietary Name | TRETIN.X |
| Package Description | 1 TUBE in 1 CARTON (16781-376-35) > 35 g in 1 TUBE |
| Product NDC | 16781-376 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRETINOIN |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130402 |
| Marketing Category Name | ANDA |
| Labeler Name | Onset Dermatologics LLC |
| Substance Name | TRETINOIN |
| Strength Number | .375 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
