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Nizatidine
Nizatidine - 21695-043-30 - (Nizatidine)
Drug Information of Nizatidine
| Product NDC: | 21695-043 |
| Proprietary Name: | Nizatidine |
| Non Proprietary Name: | Nizatidine |
| Active Ingredient(s): | 300 mg/1 & nbsp; Nizatidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nizatidine
| Product NDC: | 21695-043 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075616 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020709 |
Package Information of Nizatidine
| Package NDC: | 21695-043-30 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (21695-043-30) |
NDC Information of Nizatidine
| NDC Code | 21695-043-30 |
| Proprietary Name | Nizatidine |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (21695-043-30) |
| Product NDC | 21695-043 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nizatidine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20020709 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | NIZATIDINE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
