| NDC Code | 53002-7041-4 |
|---|
| Package Description | 20 CAPSULE in 1 BOTTLE (53002-7041-4) |
|---|
| Product NDC | 53002-7041 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Nitrofurantoin |
|---|
| Non-Proprietary Name | Nitrofurantoin (monohydrate/macrocrystals) |
|---|
| Dosage Form | CAPSULE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20050406 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077066 |
|---|
| Manufacturer | RPK Pharmaceuticals, Inc. |
|---|
| Substance Name | NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE |
|---|
| Strength | 25; 75 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Nitrofuran Antibacterial [EPC], Nitrofuran Antibacterial [EPC], Nitrofurans [CS], Nitrofurans [CS] |
|---|