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PODOFILOX
PODOFILOX - 0574-0611-05 - (PODOFILOX)
Drug Information of PODOFILOX
| Product NDC: | 0574-0611 |
| Proprietary Name: | PODOFILOX |
| Non Proprietary Name: | PODOFILOX |
| Active Ingredient(s): | 5 mg/mL & nbsp; PODOFILOX |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PODOFILOX
| Product NDC: | 0574-0611 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075600 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020129 |
Package Information of PODOFILOX
| Package NDC: | 0574-0611-05 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (0574-0611-05) > 3.5 mL in 1 BOTTLE, GLASS |
NDC Information of PODOFILOX
| NDC Code | 0574-0611-05 |
| Proprietary Name | PODOFILOX |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (0574-0611-05) > 3.5 mL in 1 BOTTLE, GLASS |
| Product NDC | 0574-0611 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PODOFILOX |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20020129 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | PODOFILOX |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Mitosis [PE] |
