Product NDC: | 67546-111 |
Proprietary Name: | Alinia |
Non Proprietary Name: | nitazoxanide |
Active Ingredient(s): | 500 mg/1 & nbsp; nitazoxanide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67546-111 |
Labeler Name: | Romark Laboratories, LC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021497 |
Marketing Category: | NDA |
Start Marketing Date: | 20040721 |
Package NDC: | 67546-111-11 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (67546-111-11) > 60 TABLET in 1 BOTTLE, PLASTIC |
NDC Code | 67546-111-11 |
Proprietary Name | Alinia |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (67546-111-11) > 60 TABLET in 1 BOTTLE, PLASTIC |
Product NDC | 67546-111 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nitazoxanide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20040721 |
Marketing Category Name | NDA |
Labeler Name | Romark Laboratories, LC |
Substance Name | NITAZOXANIDE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antiprotozoal [EPC] |