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Nitrofurantoin (monohydrate/macrocrystals)
Nitrofurantoin (monohydrate/macrocrystals) - 0185-0122-10 - (Nitrofurantoin (monohydrate/macrocrystals))
Drug Information of Nitrofurantoin (monohydrate/macrocrystals)
| Product NDC: | 0185-0122 |
| Proprietary Name: | Nitrofurantoin (monohydrate/macrocrystals) |
| Non Proprietary Name: | Nitrofurantoin (monohydrate/macrocrystals) |
| Active Ingredient(s): | 25; 75 mg/1; mg/1 & nbsp; Nitrofurantoin (monohydrate/macrocrystals) |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nitrofurantoin (monohydrate/macrocrystals)
| Product NDC: | 0185-0122 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080043 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19701125 |
Package Information of Nitrofurantoin (monohydrate/macrocrystals)
| Package NDC: | 0185-0122-10 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE (0185-0122-10) |
NDC Information of Nitrofurantoin (monohydrate/macrocrystals)
| NDC Code | 0185-0122-10 |
| Proprietary Name | Nitrofurantoin (monohydrate/macrocrystals) |
| Package Description | 1000 CAPSULE in 1 BOTTLE (0185-0122-10) |
| Product NDC | 0185-0122 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nitrofurantoin (monohydrate/macrocrystals) |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19701125 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE |
| Strength Number | 25; 75 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient],Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient] |
