Gentamicin Sulfate
- Product NDC
- 50090-0568
- 11-digit product format
- 500900568
- Labeler code
- 50090
- Product ID
- 50090-0568_061cb54c-d2cd-4b8c-a24a-07ef8bc2a6d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gentamicin Sulfate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA064163
- Marketing category
- ANDA
- Marketing start
- 2006-12-13
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0568-0 | 50090056800 | 1 BOTTLE, DROPPER in 1 CARTON (50090-0568-0) > 5 mL in 1 BOTTLE, DROPPER | 2014-11-28 | 0000-00-00 | No | No | Current |