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Nitrofurantoin
Nitrofurantoin - 49349-040-04 - (Nitrofurantoin)
Drug Information of Nitrofurantoin
| Product NDC: | 49349-040 |
| 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: | 49349-040 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073652 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111110 |
Package Information of Nitrofurantoin
| Package NDC: | 49349-040-04 |
| Package Description: | 14 CAPSULE in 1 BLISTER PACK (49349-040-04) |
NDC Information of Nitrofurantoin
| NDC Code | 49349-040-04 |
| Proprietary Name | Nitrofurantoin |
| Package Description | 14 CAPSULE in 1 BLISTER PACK (49349-040-04) |
| Product NDC | 49349-040 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nitrofurantoin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20111110 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | NITROFURANTOIN |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient] |
