Product NDC: | 0064-5010 |
Proprietary Name: | COLLAGENASE SANTYL |
Non Proprietary Name: | COLLAGENASE SANTYL |
Active Ingredient(s): | 250 [arb'U]/g & nbsp; COLLAGENASE SANTYL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0064-5010 |
Labeler Name: | HEALTHPOINT, LTD |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA101995 |
Marketing Category: | BLA |
Start Marketing Date: | 20061018 |
Package NDC: | 0064-5010-15 |
Package Description: | 1 TUBE in 1 CARTON (0064-5010-15) > 15 g in 1 TUBE |
NDC Code | 0064-5010-15 |
Proprietary Name | COLLAGENASE SANTYL |
Package Description | 1 TUBE in 1 CARTON (0064-5010-15) > 15 g in 1 TUBE |
Product NDC | 0064-5010 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | COLLAGENASE SANTYL |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20061018 |
Marketing Category Name | BLA |
Labeler Name | HEALTHPOINT, LTD |
Substance Name | COLLAGENASE CLOSTRIDIUM HISTOLYTICUM |
Strength Number | 250 |
Strength Unit | [arb'U]/g |
Pharmaceutical Classes | Collagenases [Chemical/Ingredient],Collagen-specific Enzyme [EPC] |