Gentak
- Product NDC
- 68071-1513
- 11-digit product format
- 680711513
- Labeler code
- 68071
- Product ID
- 68071-1513_bb04e9b1-559f-39d1-e053-2995a90a2158
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gentamicin Sulfate
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA064093
- Marketing category
- ANDA
- Marketing start
- 2006-05-08
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1513-5 | 68071151305 | 3.5 g in 1 BOX (68071-1513-5) | 3.5 g | 2019-02-05 | 0000-00-00 | No | No | Current |