Product NDC: | 68788-9838 |
Proprietary Name: | Nizatidine |
Non Proprietary Name: | Nizatidine |
Active Ingredient(s): | 150 mg/1 & nbsp; Nizatidine |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9838 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090618 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120329 |
Package NDC: | 68788-9838-9 |
Package Description: | 90 CAPSULE in 1 BOTTLE (68788-9838-9) |
NDC Code | 68788-9838-9 |
Proprietary Name | Nizatidine |
Package Description | 90 CAPSULE in 1 BOTTLE (68788-9838-9) |
Product NDC | 68788-9838 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nizatidine |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20120329 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | NIZATIDINE |
Strength Number | 150 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |