Product NDC: | 67546-212 |
Proprietary Name: | Alinia |
Non Proprietary Name: | nitazoxanide |
Active Ingredient(s): | 100 mg/5mL & nbsp; nitazoxanide |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67546-212 |
Labeler Name: | Romark Laboratories, LC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021498 |
Marketing Category: | NDA |
Start Marketing Date: | 20021122 |
Package NDC: | 67546-212-21 |
Package Description: | 1 BOTTLE, GLASS in 1 CARTON (67546-212-21) > 60 mL in 1 BOTTLE, GLASS |
NDC Code | 67546-212-21 |
Proprietary Name | Alinia |
Package Description | 1 BOTTLE, GLASS in 1 CARTON (67546-212-21) > 60 mL in 1 BOTTLE, GLASS |
Product NDC | 67546-212 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nitazoxanide |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20021122 |
Marketing Category Name | NDA |
Labeler Name | Romark Laboratories, LC |
Substance Name | NITAZOXANIDE |
Strength Number | 100 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Antiprotozoal [EPC] |