Product NDC: | 0168-0071 |
Proprietary Name: | Gentamicin Sulfate |
Non Proprietary Name: | gentamicin sulfate |
Active Ingredient(s): | 1 mg/g & nbsp; gentamicin sulfate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0168-0071 |
Labeler Name: | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062531 |
Marketing Category: | ANDA |
Start Marketing Date: | 19840705 |
Package NDC: | 0168-0071-15 |
Package Description: | 15 g in 1 TUBE (0168-0071-15) |
NDC Code | 0168-0071-15 |
Proprietary Name | Gentamicin Sulfate |
Package Description | 15 g in 1 TUBE (0168-0071-15) |
Product NDC | 0168-0071 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | gentamicin sulfate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19840705 |
Marketing Category Name | ANDA |
Labeler Name | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. |
Substance Name | GENTAMICIN SULFATE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |