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Alinia
Alinia - 67546-212-21 - (nitazoxanide)
Drug Information of Alinia
| 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) |
Labeler Information of Alinia
| 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 Information of Alinia
| Package NDC: | 67546-212-21 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (67546-212-21) > 60 mL in 1 BOTTLE, GLASS |
NDC Information of Alinia
| 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] |
