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DRITHO-CREME
DRITHO-CREME - 11086-037-01 - (ANTHRALIN)
Drug Information of DRITHO-CREME
| Product NDC: | 11086-037 |
| Proprietary Name: | DRITHO-CREME |
| Non Proprietary Name: | ANTHRALIN |
| Active Ingredient(s): | 1 g/100g & nbsp; ANTHRALIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DRITHO-CREME
| Product NDC: | 11086-037 |
| Labeler Name: | Summers Laboratories Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130101 |
Package Information of DRITHO-CREME
| Package NDC: | 11086-037-01 |
| Package Description: | 50 g in 1 TUBE (11086-037-01) |
NDC Information of DRITHO-CREME
| NDC Code | 11086-037-01 |
| Proprietary Name | DRITHO-CREME |
| Package Description | 50 g in 1 TUBE (11086-037-01) |
| Product NDC | 11086-037 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ANTHRALIN |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Summers Laboratories Inc |
| Substance Name | ANTHRALIN |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
