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Triamcinolone Acetonide
Triamcinolone Acetonide - 0168-0006-15 - (triamcinolone acetonide)
Drug Information of Triamcinolone Acetonide
| Product NDC: | 0168-0006 |
| Proprietary Name: | Triamcinolone Acetonide |
| Non Proprietary Name: | triamcinolone acetonide |
| Active Ingredient(s): | 1 mg/g & nbsp; triamcinolone acetonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Triamcinolone Acetonide
| Product NDC: | 0168-0006 |
| Labeler Name: | E. Fougera & CO., A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085691 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19780214 |
Package Information of Triamcinolone Acetonide
| Package NDC: | 0168-0006-15 |
| Package Description: | 15 g in 1 TUBE (0168-0006-15) |
NDC Information of Triamcinolone Acetonide
| NDC Code | 0168-0006-15 |
| Proprietary Name | Triamcinolone Acetonide |
| Package Description | 15 g in 1 TUBE (0168-0006-15) |
| Product NDC | 0168-0006 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | triamcinolone acetonide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19780214 |
| Marketing Category Name | ANDA |
| Labeler Name | E. Fougera & CO., A division of Fougera Pharmaceuticals Inc. |
| Substance Name | TRIAMCINOLONE ACETONIDE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
