Product NDC: | 54868-6203 |
Proprietary Name: | Nitrofurantoin Monohydrate/Macrocrystals |
Non Proprietary Name: | Nitrofurantoin Monohydrate and Nitrofurantoin, macrocrystalline |
Active Ingredient(s): | 25; 75 mg/1; mg/1 & nbsp; Nitrofurantoin Monohydrate and Nitrofurantoin, macrocrystalline |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6203 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076648 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110106 |
Package NDC: | 54868-6203-0 |
Package Description: | 14 CAPSULE in 1 BOTTLE, PLASTIC (54868-6203-0) |
NDC Code | 54868-6203-0 |
Proprietary Name | Nitrofurantoin Monohydrate/Macrocrystals |
Package Description | 14 CAPSULE in 1 BOTTLE, PLASTIC (54868-6203-0) |
Product NDC | 54868-6203 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nitrofurantoin Monohydrate and Nitrofurantoin, macrocrystalline |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20110106 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE |
Strength Number | 25; 75 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient],Nitrofuran Antibacterial [EPC],Nitrofurans [Chemical/Ingredient] |