Gentak
- Product NDC
- 68788-9732
- 11-digit product format
- 687889732
- Labeler code
- 68788
- Product ID
- 68788-9732_f2a19133-aa54-460e-9d4f-302d8cf32256
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gentamicin Sulfate
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA064093
- Marketing category
- ANDA
- Marketing start
- 2012-10-23
- 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
- 2021-12-31
- 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 |
|---|
| 68788-9732-3 | 68788973203 | 1 TUBE in 1 CARTON (68788-9732-3) > 3.5 g in 1 TUBE | 1 tube | 2012-10-23 | 0000-00-00 | No | No | Current |