Gentak
- Product NDC
- 17478-827
- 11-digit product format
- 174780827
- Labeler code
- 17478
- Product ID
- 17478-827_fa318f79-5dbe-4059-b6d2-c7ae32fe18bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gentamicin Sulfate
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- Akorn
- Application
- ANDA064093
- Marketing category
- ANDA
- Marketing start
- 2013-03-11
- Marketing end
- 0000-00-00
- Substance
- GENTAMICIN SULFATE
- Active strength
- 3 mg/g
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-827-35 | 17478082735 | 1 TUBE in 1 CARTON (17478-827-35) > 3.5 g in 1 TUBE | 1 tube | 2013-03-11 | 0000-00-00 | No | No | Current |