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PRED-G
PRED-G - 0023-0106-05 - (gentamicin, prednisolone acetate)
Drug Information of PRED-G
| Product NDC: | 0023-0106 |
| Proprietary Name: | PRED-G |
| Non Proprietary Name: | gentamicin, prednisolone acetate |
| Active Ingredient(s): | 3; 10 mg/mL; mg/mL & nbsp; gentamicin, prednisolone acetate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRED-G
| Product NDC: | 0023-0106 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050586 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19900219 |
Package Information of PRED-G
| Package NDC: | 0023-0106-05 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0023-0106-05) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of PRED-G
| NDC Code | 0023-0106-05 |
| Proprietary Name | PRED-G |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0023-0106-05) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0023-0106 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | gentamicin, prednisolone acetate |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19900219 |
| Marketing Category Name | NDA |
| Labeler Name | Allergan, Inc. |
| Substance Name | GENTAMICIN; PREDNISOLONE ACETATE |
| Strength Number | 3; 10 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
