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TRETIN-X
TRETIN-X - 63094-0379-3 - (Tretinoin Gel 0.01%)
Drug Information of TRETIN-X
| Product NDC: | 63094-0379 |
| Proprietary Name: | TRETIN-X |
| Non Proprietary Name: | Tretinoin Gel 0.01% |
| Active Ingredient(s): | .1 mg/g & nbsp; Tretinoin Gel 0.01% |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRETIN-X
| Product NDC: | 63094-0379 |
| Labeler Name: | DPT Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075589 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070420 |
Package Information of TRETIN-X
| Package NDC: | 63094-0379-3 |
| Package Description: | 1 TUBE in 1 CARTON (63094-0379-3) > 35 g in 1 TUBE |
NDC Information of TRETIN-X
| NDC Code | 63094-0379-3 |
| Proprietary Name | TRETIN-X |
| Package Description | 1 TUBE in 1 CARTON (63094-0379-3) > 35 g in 1 TUBE |
| Product NDC | 63094-0379 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tretinoin Gel 0.01% |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20070420 |
| Marketing Category Name | ANDA |
| Labeler Name | DPT Laboratories, Ltd. |
| Substance Name | TRETINOIN |
| Strength Number | .1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
