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Nitrofurantoin (macrocrystals)
Nitrofurantoin (macrocrystals) - 51079-584-20 - (Nitrofurantoin (macrocrystals))
Drug Information of Nitrofurantoin (macrocrystals)
| Product NDC: | 51079-584 |
| 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: | 51079-584 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074967 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110114 |
Package Information of Nitrofurantoin (macrocrystals)
| Package NDC: | 51079-584-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-584-20) > 1 CAPSULE in 1 BLISTER PACK (51079-584-01) |
NDC Information of Nitrofurantoin (macrocrystals)
| NDC Code | 51079-584-20 |
| Proprietary Name | Nitrofurantoin (macrocrystals) |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-584-20) > 1 CAPSULE in 1 BLISTER PACK (51079-584-01) |
| Product NDC | 51079-584 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nitrofurantoin (macrocrystals) |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110114 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | NITROFURANTOIN |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient] |
