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Nitrofurantoin
Nitrofurantoin - 43063-173-02 - (nitrofurantoin)
Drug Information of Nitrofurantoin
| Product NDC: | 43063-173 |
| Proprietary Name: | Nitrofurantoin |
| Non Proprietary Name: | nitrofurantoin |
| Active Ingredient(s): | 100 mg/1 & nbsp; nitrofurantoin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nitrofurantoin
| Product NDC: | 43063-173 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074967 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110506 |
Package Information of Nitrofurantoin
| Package NDC: | 43063-173-02 |
| Package Description: | 2 CAPSULE in 1 BOTTLE, PLASTIC (43063-173-02) |
NDC Information of Nitrofurantoin
| NDC Code | 43063-173-02 |
| Proprietary Name | Nitrofurantoin |
| Package Description | 2 CAPSULE in 1 BOTTLE, PLASTIC (43063-173-02) |
| Product NDC | 43063-173 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nitrofurantoin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110506 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | NITROFURANTOIN |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient] |
