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TACLONEX SCALP
TACLONEX SCALP - 0430-3240-96 - (calcipotriene 0.005% and betamethasone dipropionate 0.064%)
Drug Information of TACLONEX SCALP
| Product NDC: | 0430-3240 |
| Proprietary Name: | TACLONEX SCALP |
| Non Proprietary Name: | calcipotriene 0.005% and betamethasone dipropionate 0.064% |
| Active Ingredient(s): | .643; 50 mg/g; ug/g & nbsp; calcipotriene 0.005% and betamethasone dipropionate 0.064% |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TACLONEX SCALP
| Product NDC: | 0430-3240 |
| Labeler Name: | Warner Chilcott (US), LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022185 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080601 |
Package Information of TACLONEX SCALP
| Package NDC: | 0430-3240-96 |
| Package Description: | 40 CARTON in 1 CASE (0430-3240-96) > 1 BOTTLE in 1 CARTON > 4 g in 1 BOTTLE |
NDC Information of TACLONEX SCALP
| NDC Code | 0430-3240-96 |
| Proprietary Name | TACLONEX SCALP |
| Package Description | 40 CARTON in 1 CASE (0430-3240-96) > 1 BOTTLE in 1 CARTON > 4 g in 1 BOTTLE |
| Product NDC | 0430-3240 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | calcipotriene 0.005% and betamethasone dipropionate 0.064% |
| Dosage Form Name | SPRAY, METERED |
| Route Name | TOPICAL |
| Start Marketing Date | 20080601 |
| Marketing Category Name | NDA |
| Labeler Name | Warner Chilcott (US), LLC |
| Substance Name | BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE |
| Strength Number | .643; 50 |
| Strength Unit | mg/g; ug/g |
| Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |
