| Product NDC: | 54569-0181 |
| 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) |
| Product NDC: | 54569-0181 |
| Labeler Name: | A-S Medication Solutions LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074967 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121024 |
| Package NDC: | 54569-0181-0 |
| Package Description: | 28 CAPSULE in 1 BOTTLE, PLASTIC (54569-0181-0) |
| NDC Code | 54569-0181-0 |
| Proprietary Name | Nitrofurantoin (macrocrystals) |
| Package Description | 28 CAPSULE in 1 BOTTLE, PLASTIC (54569-0181-0) |
| Product NDC | 54569-0181 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nitrofurantoin (macrocrystals) |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20121024 |
| Marketing Category Name | ANDA |
| Labeler Name | A-S Medication Solutions LLC |
| Substance Name | NITROFURANTOIN |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient] |