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Nitrofurantoin Macrocrystals
Nitrofurantoin Macrocrystals - 0093-2130-10 - (Nitrofurantoin Macrocrystals)
Drug Information of Nitrofurantoin Macrocrystals
| Product NDC: | 0093-2130 |
| Proprietary Name: | Nitrofurantoin Macrocrystals |
| Non Proprietary Name: | Nitrofurantoin Macrocrystals |
| Active Ingredient(s): | 50 mg/1 & nbsp; Nitrofurantoin Macrocrystals |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nitrofurantoin Macrocrystals
| Product NDC: | 0093-2130 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073671 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070308 |
Package Information of Nitrofurantoin Macrocrystals
| Package NDC: | 0093-2130-10 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE (0093-2130-10) |
NDC Information of Nitrofurantoin Macrocrystals
| NDC Code | 0093-2130-10 |
| Proprietary Name | Nitrofurantoin Macrocrystals |
| Package Description | 1000 CAPSULE in 1 BOTTLE (0093-2130-10) |
| Product NDC | 0093-2130 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nitrofurantoin Macrocrystals |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20070308 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | NITROFURANTOIN |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient] |
