TOBRAMYCIN AND DEXAMETHASONE
- Product NDC
- 71335-2840
- 11-digit product format
- 713352840
- Labeler code
- 71335
- Product ID
- 71335-2840_0ca84757-3322-4341-9246-6612758af09d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tobramycin and dexamethasone
- Dosage form
- SUSPENSION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212715
- Marketing category
- ANDA
- Marketing start
- 2022-03-17
- Substance
- DEXAMETHASONE; TOBRAMYCIN
- Active strength
- 1; 3 mg/mL; mg/mL
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7S5I7G3JQL | DEXAMETHASONE | 50-02-2 | DEXAMETHASONE |
| VZ8RRZ51VK | TOBRAMYCIN | 32986-56-4 | TOBRAMYCIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2840-1 | 71335284001 | 5 mL in 1 BOTTLE, PLASTIC (71335-2840-1) | 5 ml | 2025-10-21 | No | No | Historical |