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Gentak
Gentak - 52125-296-01 - (Gentamicin Sulfate)
Drug Information of Gentak
| Product NDC: | 52125-296 |
| Proprietary Name: | Gentak |
| Non Proprietary Name: | Gentamicin Sulfate |
| Active Ingredient(s): | 3 mg/g & nbsp; Gentamicin Sulfate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gentak
| Product NDC: | 52125-296 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064093 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130624 |
Package Information of Gentak
| Package NDC: | 52125-296-01 |
| Package Description: | 3.5 g in 1 TUBE (52125-296-01) |
NDC Information of Gentak
| NDC Code | 52125-296-01 |
| Proprietary Name | Gentak |
| Package Description | 3.5 g in 1 TUBE (52125-296-01) |
| Product NDC | 52125-296 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Gentamicin Sulfate |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20130624 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 3 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
