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Nitrofurantoin
Nitrofurantoin - 65162-689-88 - (Nitrofurantoin)
Drug Information of Nitrofurantoin
| Product NDC: | 65162-689 |
| Proprietary Name: | Nitrofurantoin |
| Non Proprietary Name: | Nitrofurantoin |
| Active Ingredient(s): | 25 mg/5mL & nbsp; Nitrofurantoin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nitrofurantoin
| Product NDC: | 65162-689 |
| Labeler Name: | Amneal Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201679 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110324 |
Package Information of Nitrofurantoin
| Package NDC: | 65162-689-88 |
| Package Description: | 230 mL in 1 BOTTLE, GLASS (65162-689-88) |
NDC Information of Nitrofurantoin
| NDC Code | 65162-689-88 |
| Proprietary Name | Nitrofurantoin |
| Package Description | 230 mL in 1 BOTTLE, GLASS (65162-689-88) |
| Product NDC | 65162-689 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nitrofurantoin |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20110324 |
| Marketing Category Name | ANDA |
| Labeler Name | Amneal Pharmaceuticals |
| Substance Name | NITROFURANTOIN |
| Strength Number | 25 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient] |
