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Synalar
Synalar - 43538-901-12 - (Fluocinolone acetonide)
Drug Information of Synalar
| Product NDC: | 43538-901 |
| Proprietary Name: | Synalar |
| Non Proprietary Name: | Fluocinolone acetonide |
| Active Ingredient(s): | & nbsp; Fluocinolone acetonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Synalar
| Product NDC: | 43538-901 |
| Labeler Name: | Medimetriks Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012787 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121215 |
Package Information of Synalar
| Package NDC: | 43538-901-12 |
| Package Description: | 1 KIT in 1 CARTON (43538-901-12) * 1 TUBE in 1 CARTON > 120 g in 1 TUBE * 255 g in 1 TUBE |
NDC Information of Synalar
| NDC Code | 43538-901-12 |
| Proprietary Name | Synalar |
| Package Description | 1 KIT in 1 CARTON (43538-901-12) * 1 TUBE in 1 CARTON > 120 g in 1 TUBE * 255 g in 1 TUBE |
| Product NDC | 43538-901 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluocinolone acetonide |
| Dosage Form Name | KIT |
| Route Name | TOPICAL |
| Start Marketing Date | 20121215 |
| Marketing Category Name | NDA |
| Labeler Name | Medimetriks Pharmaceuticals, Inc. |
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