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PRED-G
PRED-G - 0023-0066-04 - (gentamicin sulfate and prednisolone acetate)
Drug Information of PRED-G
| Product NDC: | 0023-0066 |
| Proprietary Name: | PRED-G |
| Non Proprietary Name: | gentamicin sulfate and prednisolone acetate |
| Active Ingredient(s): | 3; 6 mg/g; mg/g & nbsp; gentamicin sulfate and prednisolone acetate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRED-G
| Product NDC: | 0023-0066 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050612 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19900101 |
Package Information of PRED-G
| Package NDC: | 0023-0066-04 |
| Package Description: | 1 TUBE in 1 CARTON (0023-0066-04) > 3.5 g in 1 TUBE |
NDC Information of PRED-G
| NDC Code | 0023-0066-04 |
| Proprietary Name | PRED-G |
| Package Description | 1 TUBE in 1 CARTON (0023-0066-04) > 3.5 g in 1 TUBE |
| Product NDC | 0023-0066 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | gentamicin sulfate and prednisolone acetate |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19900101 |
| Marketing Category Name | NDA |
| Labeler Name | Allergan, Inc. |
| Substance Name | GENTAMICIN SULFATE; PREDNISOLONE ACETATE |
| Strength Number | 3; 6 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
