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Tretinoin
Tretinoin - 21695-655-20 - (tretinoin)
Drug Information of Tretinoin
| Product NDC: | 21695-655 |
| Proprietary Name: | Tretinoin |
| 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 Tretinoin
| Product NDC: | 21695-655 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075264 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981224 |
Package Information of Tretinoin
| Package NDC: | 21695-655-20 |
| Package Description: | 1 TUBE in 1 CARTON (21695-655-20) > 20 g in 1 TUBE |
NDC Information of Tretinoin
| NDC Code | 21695-655-20 |
| Proprietary Name | Tretinoin |
| Package Description | 1 TUBE in 1 CARTON (21695-655-20) > 20 g in 1 TUBE |
| Product NDC | 21695-655 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tretinoin |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19981224 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | TRETINOIN |
| Strength Number | .25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
