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Nizatidine
Nizatidine - 65162-659-90 - (Nizatidine)
Drug Information of Nizatidine
| Product NDC: | 65162-659 |
| Proprietary Name: | Nizatidine |
| Non Proprietary Name: | Nizatidine |
| Active Ingredient(s): | 15 mg/mL & nbsp; Nizatidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nizatidine
| Product NDC: | 65162-659 |
| Labeler Name: | Amneal Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090576 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091214 |
Package Information of Nizatidine
| Package NDC: | 65162-659-90 |
| Package Description: | 480 mL in 1 BOTTLE (65162-659-90) |
NDC Information of Nizatidine
| NDC Code | 65162-659-90 |
| Proprietary Name | Nizatidine |
| Package Description | 480 mL in 1 BOTTLE (65162-659-90) |
| Product NDC | 65162-659 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nizatidine |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20091214 |
| Marketing Category Name | ANDA |
| Labeler Name | Amneal Pharmaceuticals |
| Substance Name | NIZATIDINE |
| Strength Number | 15 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
