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Ultravate X
Ultravate X - 10631-121-01 - (Halobetasol Propionate)
Drug Information of Ultravate X
| Product NDC: | 10631-121 |
| Proprietary Name: | Ultravate X |
| Non Proprietary Name: | Halobetasol Propionate |
| Active Ingredient(s): | & nbsp; Halobetasol Propionate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultravate X
| Product NDC: | 10631-121 |
| Labeler Name: | Ranbaxy Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019967 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120709 |
Package Information of Ultravate X
| Package NDC: | 10631-121-01 |
| Package Description: | 1 KIT in 1 CARTON (10631-121-01) * 50 g in 1 TUBE (10631-103-50) * 225 g in 1 TUBE (10631-114-05) |
NDC Information of Ultravate X
| NDC Code | 10631-121-01 |
| Proprietary Name | Ultravate X |
| Package Description | 1 KIT in 1 CARTON (10631-121-01) * 50 g in 1 TUBE (10631-103-50) * 225 g in 1 TUBE (10631-114-05) |
| Product NDC | 10631-121 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Halobetasol Propionate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120709 |
| Marketing Category Name | NDA |
| Labeler Name | Ranbaxy Laboratories Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
