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Famotidine
Famotidine - 43386-500-11 - (Famotidine)
Drug Information of Famotidine
| Product NDC: | 43386-500 |
| Proprietary Name: | Famotidine |
| Non Proprietary Name: | Famotidine |
| Active Ingredient(s): | 40 mg/5mL & nbsp; Famotidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Famotidine
| Product NDC: | 43386-500 |
| Labeler Name: | GAVIS Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201695 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121217 |
Package Information of Famotidine
| Package NDC: | 43386-500-11 |
| Package Description: | 50 mL in 1 BOTTLE (43386-500-11) |
NDC Information of Famotidine
| NDC Code | 43386-500-11 |
| Proprietary Name | Famotidine |
| Package Description | 50 mL in 1 BOTTLE (43386-500-11) |
| Product NDC | 43386-500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20121217 |
| Marketing Category Name | ANDA |
| Labeler Name | GAVIS Pharmaceuticals, LLC |
| Substance Name | FAMOTIDINE |
| Strength Number | 40 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
