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Nizatidine
Nizatidine - 55111-310-05 - (Nizatidine)
Drug Information of Nizatidine
| Product NDC: | 55111-310 |
| 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) |
Labeler Information of Nizatidine
| Product NDC: | 55111-310 |
| Labeler Name: | Dr Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077314 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050915 |
Package Information of Nizatidine
| Package NDC: | 55111-310-05 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (55111-310-05) |
NDC Information of Nizatidine
| NDC Code | 55111-310-05 |
| Proprietary Name | Nizatidine |
| Package Description | 500 CAPSULE in 1 BOTTLE (55111-310-05) |
| Product NDC | 55111-310 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nizatidine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20050915 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr Reddy's Laboratories Limited |
| Substance Name | NIZATIDINE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
