GENTAMICIN SULFATE
- Product NDC
- 68788-9921
- 11-digit product format
- 687889921
- Labeler code
- 68788
- Product ID
- 68788-9921_67d124b5-29cf-45b8-818b-e807ebfcdac3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gentamicin sulfate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA062452
- Marketing category
- ANDA
- Marketing start
- 2014-03-25
- Marketing end
- 0000-00-00
- Substance
- GENTAMICIN SULFATE
- 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