Search by Drug Name or NDC
NDC 50090-1135-00 Tobramycin and Dexamethasone 1; 3 mg/mL; mg/mL Details
Tobramycin and Dexamethasone 1; 3 mg/mL; mg/mL
Tobramycin and Dexamethasone is a OPHTHALMIC SUSPENSION/ DROPS in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is DEXAMETHASONE; TOBRAMYCIN.
MedlinePlus Drug Summary
Dexamethasone reduces the irritation, redness, burning, and swelling of eye caused by chemicals, heat, radiation, infection, allergy, or foreign bodies in the eye. It is sometimes used after eye surgery.
Related Packages: 50090-1135-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Dexamethasone Ophthalmic
Ophthalmic tobramycin is used to treat eye infections. Tobramycin is in a class of medications called antibiotics. It works by killing bacteria that cause infections.
Related Packages: 50090-1135-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Tobramycin Ophthalmic
Product Information
| NDC | 50090-1135 |
|---|---|
| Product ID | 50090-1135_3ae18ae8-7fe7-4f51-86d5-25d847181f3f |
| Associated GPIs | 86309902801820 |
| GCN Sequence Number | 007986 |
| GCN Sequence Number Description | tobramycin/dexamethasone DROPS SUSP 0.3 %-0.1% OPHTHALMIC |
| HIC3 | Q6I |
| HIC3 Description | EYE ANTIBIOTIC AND GLUCOCORTICOID COMBINATIONS |
| GCN | 92280 |
| HICL Sequence Number | 039399 |
| HICL Sequence Number Description | TOBRAMYCIN/DEXAMETHASONE |
| Brand/Generic | Generic |
| Proprietary Name | Tobramycin and Dexamethasone |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Tobramycin and Dexamethasone |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SUSPENSION/ DROPS |
| Route | OPHTHALMIC |
| Active Ingredient Strength | 1; 3 |
| Active Ingredient Units | mg/mL; mg/mL |
| Substance Name | DEXAMETHASONE; TOBRAMYCIN |
| Labeler Name | A-S Medication Solutions |
| Pharmaceutical Class | Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA050592 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-1135-00 (50090113500)
| NDC Package Code | 50090-1135-0 |
|---|---|
| Billing NDC | 50090113500 |
| Package | 2.5 mL in 1 BOTTLE (50090-1135-0) |
| Marketing Start Date | 2014-11-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |