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CICLOPIROX OLAMINE
CICLOPIROX OLAMINE - 49999-646-15 - (CICLOPIROX OLAMINE)
Drug Information of CICLOPIROX OLAMINE
| Product NDC: | 49999-646 |
| Proprietary Name: | CICLOPIROX OLAMINE |
| Non Proprietary Name: | CICLOPIROX OLAMINE |
| Active Ingredient(s): | 7.7 mg/g & nbsp; CICLOPIROX OLAMINE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CICLOPIROX OLAMINE
| Product NDC: | 49999-646 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077364 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101103 |
Package Information of CICLOPIROX OLAMINE
| Package NDC: | 49999-646-15 |
| Package Description: | 15 g in 1 TUBE (49999-646-15) |
NDC Information of CICLOPIROX OLAMINE
| NDC Code | 49999-646-15 |
| Proprietary Name | CICLOPIROX OLAMINE |
| Package Description | 15 g in 1 TUBE (49999-646-15) |
| Product NDC | 49999-646 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CICLOPIROX OLAMINE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101103 |
| Marketing Category Name | ANDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | CICLOPIROX OLAMINE |
| Strength Number | 7.7 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA] |
