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Capex
Capex - 0299-5500-04 - (fluocinolone acetonide)
Drug Information of Capex
| Product NDC: | 0299-5500 |
| Proprietary Name: | Capex |
| Non Proprietary Name: | fluocinolone acetonide |
| Active Ingredient(s): | & nbsp; fluocinolone acetonide |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Capex
| Product NDC: | 0299-5500 |
| Labeler Name: | Galderma Laboratories, L.P. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020001 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19841012 |
Package Information of Capex
| Package NDC: | 0299-5500-04 |
| Package Description: | 1 KIT in 1 CARTON (0299-5500-04) * 12 mg in 1 PACKAGE * 118 mL in 1 BOTTLE |
NDC Information of Capex
| NDC Code | 0299-5500-04 |
| Proprietary Name | Capex |
| Package Description | 1 KIT in 1 CARTON (0299-5500-04) * 12 mg in 1 PACKAGE * 118 mL in 1 BOTTLE |
| Product NDC | 0299-5500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluocinolone acetonide |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19841012 |
| Marketing Category Name | NDA |
| Labeler Name | Galderma Laboratories, L.P. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
