Tobramycin
- Product NDC
- 50436-7392
- 11-digit product format
- 504367392
- Labeler code
- 50436
- Product ID
- 50436-7392_73074e65-e6e6-44a9-a959-7cf0a5c62268
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tobramycin
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Unit Dose Services
- Application
- ANDA062535
- Marketing category
- ANDA
- Marketing start
- 1995-01-09
- Marketing end
- 0000-00-00
- Substance
- TOBRAMYCIN
- Active strength
- 3 mg/mL
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record