MAXITROL
- Product NDC
- 66758-070
- 11-digit product format
- 667580070
- Labeler code
- 66758
- Product ID
- 66758-070_67c1198f-4925-4e0f-a788-bbdf86abedeb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- neomycin sulfate, polymyxin b sulfate and dexamethasone
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- Sandoz Inc
- Application
- NDA050065
- Marketing category
- NDA
- Marketing start
- 1972-01-17
- Marketing end
- 2027-05-31
- Substance
- DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
- Active strength
- 1; 3.5; 10000 mg/g; mg/g; [USP'U]/g
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7S5I7G3JQL | DEXAMETHASONE | 50-02-2 | DEXAMETHASONE |
| 057Y626693 | NEOMYCIN SULFATE | 1405-10-3 | NEOMYCIN SULFATE |
| 19371312D4 | POLYMYXIN B SULFATE | 1405-20-5 | POLYMYXIN B SULFATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66758-070-38 | 66758007038 | 3.5 g in 1 TUBE (66758-070-38) | 3.5 g | 2024-09-02 | 2027-05-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Maxitrol Ointment | Sandoz Inc | 2023-12-29 | HUMAN PRESCRIPTION DRUG LABEL | 2 |