Neomycin and Polymyxin B Sulfates and Hydrocortisone
- Product NDC
- 50436-0737
- 11-digit product format
- 504360737
- Labeler code
- 50436
- Product ID
- 50436-0737_62715127-8097-4344-bed0-d63518d2a935
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Neomycin sulfate, Polymyxin B Sulfate and Hydrocortisone
- Dosage form
- SUSPENSION/ DROPS
- Route
- AURICULAR (OTIC)
- Labeler
- Unit Dose Services
- Application
- ANDA064065
- Marketing category
- ANDA
- Marketing start
- 1996-08-28
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
- Active strength
- 10 mg/mL; mg/mL; [USP'U]/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS],Polymyxin-class Antibacterial [EPC],Polymyxins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record