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ZITHRANOL-RR
ZITHRANOL-RR - 42783-101-15 - (anthralin)
Drug Information of ZITHRANOL-RR
| Product NDC: | 42783-101 |
| Proprietary Name: | ZITHRANOL-RR |
| Non Proprietary Name: | anthralin |
| Active Ingredient(s): | .012 g/g & nbsp; anthralin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZITHRANOL-RR
| Product NDC: | 42783-101 |
| Labeler Name: | Elorac Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090709 |
Package Information of ZITHRANOL-RR
| Package NDC: | 42783-101-15 |
| Package Description: | 6 TUBE in 1 CARTON (42783-101-15) > 15 g in 1 TUBE |
NDC Information of ZITHRANOL-RR
| NDC Code | 42783-101-15 |
| Proprietary Name | ZITHRANOL-RR |
| Package Description | 6 TUBE in 1 CARTON (42783-101-15) > 15 g in 1 TUBE |
| Product NDC | 42783-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | anthralin |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090709 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Elorac Inc. |
| Substance Name | ANTHRALIN |
| Strength Number | .012 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
