Gentamicin Sulfate
- Product NDC
- 17478-826
- 11-digit product format
- 174780826
- Labeler code
- 17478
- Product ID
- 17478-826_cf06070a-4d1d-47d1-b5a5-f83c4fd458d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gentamicin Sulfate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Akorn
- Application
- ANDA064163
- Marketing category
- ANDA
- Marketing start
- 2013-03-11
- 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
- 2023-12-31
- 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 |
|---|
| 17478-826-05 | 17478082605 | 1 BOTTLE, DROPPER in 1 CARTON (17478-826-05) > 5 mL in 1 BOTTLE, DROPPER | 2013-03-11 | 0000-00-00 | No | No | Current |